Canonical Allele Identifier: CA631300632
Gene: GAMT HGNC NCBI

Linked Data

dbSNP Id: rs1437301660

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399063del , CM000681.2:g.1399063del GRCh38
NC_000019.9:g.1399062del , CM000681.1:g.1399062del GRCh37
NC_000019.8:g.1350062del NCBI36
NG_009785.1:g.7491del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.460-37del MANE Select ENSP00000252288.1:n.460-37del
ENST00000447102.8:c.460-37del ENSP00000403536.2:n.460-37del
ENST00000591788.3:c.143-37del
ENST00000640164.1:n.293-37del
ENST00000640762.1:c.391-37del ENSP00000492031.1:n.391-37del
ENST00000252288.6:c.460-37del ENSP00000252288.1:n.460-37del
ENST00000447102.7:c.460-37del ENSP00000403536.2:n.460-37del
ENST00000591788.2:c.145-37del ENSP00000466341.2:n.145-37del
NM_000156.5:c.460-37del NP_000147.1:n.460-37del
NM_138924.2:c.460-37del NP_620279.1:n.460-37del
NM_000156.6:c.460-37del MANE Select NP_000147.1:n.460-37del
NM_138924.3:c.460-37del NP_620279.1:n.460-37del