Canonical Allele Identifier: CA341324779
Gene: AGL HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.100356774A>C (hg19) chr1:g.99891218A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99891218A>C , CM000663.2:g.99891218A>C GRCh38
NC_000001.10:g.100356774A>C , CM000663.1:g.100356774A>C GRCh37
NC_000001.9:g.100129362A>C NCBI36
NG_012865.1:g.46135A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.2813-2A>C MANE Select ENSP00000355106.3:n.2813-2A>C
ENST00000637337.1:n.3024-2A>C
ENST00000294724.8:c.2813-2A>C ENSP00000294724.4:n.2813-2A>C
ENST00000361302.7:c.2765-2A>C ENSP00000354971.3:n.2765-2A>C
ENST00000361522.4:c.2762-2A>C ENSP00000354635.4:n.2762-2A>C
ENST00000361915.7:c.2813-2A>C ENSP00000355106.3:n.2813-2A>C
ENST00000370161.6:c.2765-2A>C ENSP00000359180.2:n.2765-2A>C
ENST00000370163.7:c.2813-2A>C ENSP00000359182.3:n.2813-2A>C
ENST00000370165.7:c.2813-2A>C ENSP00000359184.3:n.2813-2A>C
NM_000028.2:c.2813-2A>C NP_000019.2:n.2813-2A>C
NM_000642.2:c.2813-2A>C NP_000633.2:n.2813-2A>C
NM_000643.2:c.2813-2A>C NP_000634.2:n.2813-2A>C
NM_000644.2:c.2813-2A>C NP_000635.2:n.2813-2A>C
NM_000645.2:c.2762-2A>C NP_000636.2:n.2762-2A>C
NM_000646.2:c.2765-2A>C NP_000637.2:n.2765-2A>C
XM_005270557.1:c.2813-2A>C XP_005270614.1:n.2813-2A>C
XM_005270557.2:c.2813-2A>C XP_005270614.1:n.2813-2A>C
XM_017000501.2:c.1073-2A>C XP_016855990.1:n.1073-2A>C
NM_000642.3:c.2813-2A>C MANE Select NP_000633.2:n.2813-2A>C
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