Canonical Allele Identifier: CA402994798
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1399026C>G (hg19) chr19:g.1399027C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399027C>G , CM000681.2:g.1399027C>G GRCh38
NC_000019.9:g.1399026C>G , CM000681.1:g.1399026C>G GRCh37
NC_000019.8:g.1350026C>G NCBI36
NG_009785.1:g.7527G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.460-1G>C MANE Select ENSP00000252288.1:n.460-1G>C
ENST00000447102.8:c.460-1G>C ENSP00000403536.2:n.460-1G>C
ENST00000591788.3:c.143-1G>C
ENST00000640164.1:n.293-1G>C
ENST00000640762.1:c.391-1G>C ENSP00000492031.1:n.391-1G>C
ENST00000252288.6:c.460-1G>C ENSP00000252288.1:n.460-1G>C
ENST00000447102.7:c.460-1G>C ENSP00000403536.2:n.460-1G>C
ENST00000591788.2:c.145-1G>C ENSP00000466341.2:n.145-1G>C
NM_000156.5:c.460-1G>C NP_000147.1:n.460-1G>C
NM_138924.2:c.460-1G>C NP_620279.1:n.460-1G>C
NM_000156.6:c.460-1G>C MANE Select NP_000147.1:n.460-1G>C
NM_138924.3:c.460-1G>C NP_620279.1:n.460-1G>C
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