Canonical Allele Identifier: CA631044739
Gene: GAMT HGNC NCBI

Linked Data

dbSNP Id: rs1227405594

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399270dup , CM000681.2:g.1399270dup GRCh38
NC_000019.9:g.1399269dup , CM000681.1:g.1399269dup GRCh37
NC_000019.8:g.1350269dup NCBI36
NG_009785.1:g.7288dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.392-71dup MANE Select ENSP00000252288.1:n.392-71dup
ENST00000447102.8:c.392-71dup ENSP00000403536.2:n.392-71dup
ENST00000591788.3:c.75-71dup
ENST00000640164.1:n.225-71dup
ENST00000640762.1:c.323-71dup ENSP00000492031.1:n.323-71dup
ENST00000252288.6:c.392-71dup ENSP00000252288.1:n.392-71dup
ENST00000447102.7:c.392-71dup ENSP00000403536.2:n.392-71dup
ENST00000591788.2:c.77-71dup ENSP00000466341.2:n.77-71dup
NM_000156.5:c.392-71dup NP_000147.1:n.392-71dup
NM_138924.2:c.392-71dup NP_620279.1:n.392-71dup
NM_000156.6:c.392-71dup MANE Select NP_000147.1:n.392-71dup
NM_138924.3:c.392-71dup NP_620279.1:n.392-71dup