Canonical Allele Identifier: CA402994776
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1399022G>T (hg19) chr19:g.1399023G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399023G>T , CM000681.2:g.1399023G>T GRCh38
NC_000019.9:g.1399022G>T , CM000681.1:g.1399022G>T GRCh37
NC_000019.8:g.1350022G>T NCBI36
NG_009785.1:g.7531C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.463C>A MANE Select ENSP00000252288.1:p.His155Asn
ENST00000447102.8:c.463C>A ENSP00000403536.2:p.His155Asn
ENST00000591788.3:c.146C>A
ENST00000640164.1:n.296C>A
ENST00000640762.1:c.394C>A ENSP00000492031.1:p.His132Asn
ENST00000252288.6:c.463C>A ENSP00000252288.1:p.His155Asn
ENST00000447102.7:c.463C>A ENSP00000403536.2:p.His155Asn
ENST00000591788.2:c.148C>A ENSP00000466341.2:p.His50Asn
NM_000156.5:c.463C>A NP_000147.1:p.His155Asn
NM_138924.2:c.463C>A NP_620279.1:p.His155Asn
NM_000156.6:c.463C>A MANE Select NP_000147.1:p.His155Asn
NM_138924.3:c.463C>A NP_620279.1:p.His155Asn
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