Canonical Allele Identifier: CA2317700309
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401197C= , CM000681.2:g.1401197C= GRCh38
NC_000019.9:g.1401196C= , CM000681.1:g.1401196C= GRCh37
NC_000019.8:g.1352196C= NCBI36
NG_009785.1:g.5357G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.181+99G= MANE Select ENSP00000252288.1:n.181+99G=
ENST00000447102.8:c.181+99G= ENSP00000403536.2:n.181+99G=
ENST00000640762.1:c.112+168G= ENSP00000492031.1:n.112+168G=
ENST00000252288.6:c.181+99G= ENSP00000252288.1:n.181+99G=
ENST00000447102.7:c.181+99G= ENSP00000403536.2:n.181+99G=
NM_000156.5:c.181+99G= NP_000147.1:n.181+99G=
NM_138924.2:c.181+99G= NP_620279.1:n.181+99G=
NM_000156.6:c.181+99G= MANE Select NP_000147.1:n.181+99G=
NM_138924.3:c.181+99G= NP_620279.1:n.181+99G=