Canonical Allele Identifier: CA2317699136
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399173T= , CM000681.2:g.1399173T= GRCh38
NC_000019.9:g.1399172T= , CM000681.1:g.1399172T= GRCh37
NC_000019.8:g.1350172T= NCBI36
NG_009785.1:g.7381A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.414A= MANE Select ENSP00000252288.1:p.Pro138=
ENST00000447102.8:c.414A= ENSP00000403536.2:p.Pro138=
ENST00000591788.3:c.97A=
ENST00000640164.1:n.247A=
ENST00000640762.1:c.345A= ENSP00000492031.1:p.Pro115=
ENST00000252288.6:c.414A= ENSP00000252288.1:p.Pro138=
ENST00000447102.7:c.414A= ENSP00000403536.2:p.Pro138=
ENST00000591788.2:c.99A= ENSP00000466341.2:p.Pro33=
NM_000156.5:c.414A= NP_000147.1:p.Pro138=
NM_138924.2:c.414A= NP_620279.1:p.Pro138=
NM_000156.6:c.414A= MANE Select NP_000147.1:p.Pro138=
NM_138924.3:c.414A= NP_620279.1:p.Pro138=