Canonical Allele Identifier: CA504895168
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1398999C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399000C>A , CM000681.2:g.1399000C>A GRCh38
NC_000019.9:g.1398999C>A , CM000681.1:g.1398999C>A GRCh37
NC_000019.8:g.1349999C>A NCBI36
NG_009785.1:g.7554G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.486G>T MANE Select ENSP00000252288.1:p.Pro162=
ENST00000447102.8:c.486G>T ENSP00000403536.2:p.Pro162=
ENST00000591788.3:c.169G>T
ENST00000640164.1:n.319G>T
ENST00000640762.1:c.417G>T ENSP00000492031.1:p.Pro139=
ENST00000252288.6:c.486G>T ENSP00000252288.1:p.Pro162=
ENST00000447102.7:c.486G>T ENSP00000403536.2:p.Pro162=
ENST00000591788.2:c.171G>T ENSP00000466341.2:p.Pro57=
NM_000156.5:c.486G>T NP_000147.1:p.Pro162=
NM_138924.2:c.486G>T NP_620279.1:p.Pro162=
NM_000156.6:c.486G>T MANE Select NP_000147.1:p.Pro162=
NM_138924.3:c.486G>T NP_620279.1:p.Pro162=
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