Canonical Allele Identifier: CA402996441
Gene: GAMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399848C>G , CM000681.2:g.1399848C>G GRCh38
NC_000019.9:g.1399847C>G , CM000681.1:g.1399847C>G GRCh37
NC_000019.8:g.1350847C>G NCBI36
NG_009785.1:g.6706G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.272G>C MANE Select ENSP00000252288.1:p.Cys91Ser
ENST00000447102.8:c.272G>C ENSP00000403536.2:p.Cys91Ser
ENST00000640762.1:c.203G>C ENSP00000492031.1:p.Cys68Ser
ENST00000252288.6:c.272G>C ENSP00000252288.1:p.Cys91Ser
ENST00000447102.7:c.272G>C ENSP00000403536.2:p.Cys91Ser
NM_000156.5:c.272G>C NP_000147.1:p.Cys91Ser
NM_138924.2:c.272G>C NP_620279.1:p.Cys91Ser
NM_000156.6:c.272G>C MANE Select NP_000147.1:p.Cys91Ser
NM_138924.3:c.272G>C NP_620279.1:p.Cys91Ser