Canonical Allele Identifier: CA2317700414
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401359G= , CM000681.2:g.1401359G= GRCh38
NC_000019.9:g.1401358G= , CM000681.1:g.1401358G= GRCh37
NC_000019.8:g.1352358G= NCBI36
NG_009785.1:g.5195C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.118C= MANE Select ENSP00000252288.1:p.Pro40=
ENST00000447102.8:c.118C= ENSP00000403536.2:p.Pro40=
ENST00000640762.1:c.112+6C= ENSP00000492031.1:n.112+6C=
ENST00000252288.6:c.118C= ENSP00000252288.1:p.Pro40=
ENST00000447102.7:c.118C= ENSP00000403536.2:p.Pro40=
NM_000156.5:c.118C= NP_000147.1:p.Pro40=
NM_138924.2:c.118C= NP_620279.1:p.Pro40=
NM_000156.6:c.118C= MANE Select NP_000147.1:p.Pro40=
NM_138924.3:c.118C= NP_620279.1:p.Pro40=