Canonical Allele Identifier: CA402994784
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 544260
ClinVar RCV Id: RCV000655366 RCV001766428 RCV001829817
dbSNP Id: rs748256259
gnomAD v2: 19-1399023-G-C
gnomAD v3: 19-1399024-G-C
gnomAD v4: 19-1399024-G-C
MyVariant Identifiers: chr19:g.1399023G>C (hg19) chr19:g.1399024G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399024G>C , CM000681.2:g.1399024G>C GRCh38
NC_000019.9:g.1399023G>C , CM000681.1:g.1399023G>C GRCh37
NC_000019.8:g.1350023G>C NCBI36
NG_009785.1:g.7530C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.462C>G MANE Select ENSP00000252288.1:p.Asn154Lys
ENST00000447102.8:c.462C>G ENSP00000403536.2:p.Asn154Lys
ENST00000591788.3:c.145C>G
ENST00000640164.1:n.295C>G
ENST00000640762.1:c.393C>G ENSP00000492031.1:p.Asn131Lys
ENST00000252288.6:c.462C>G ENSP00000252288.1:p.Asn154Lys
ENST00000447102.7:c.462C>G ENSP00000403536.2:p.Asn154Lys
ENST00000591788.2:c.147C>G ENSP00000466341.2:p.Asn49Lys
NM_000156.5:c.462C>G NP_000147.1:p.Asn154Lys
NM_138924.2:c.462C>G NP_620279.1:p.Asn154Lys
NM_000156.6:c.462C>G MANE Select NP_000147.1:p.Asn154Lys
NM_138924.3:c.462C>G NP_620279.1:p.Asn154Lys
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