Canonical Allele Identifier: CA2317698931
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398784C= , CM000681.2:g.1398784C= GRCh38
NC_000019.9:g.1398783C= , CM000681.1:g.1398783C= GRCh37
NC_000019.8:g.1349783C= NCBI36
NG_009785.1:g.7770G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.570+132G= MANE Select ENSP00000252288.1:n.570+132G=
ENST00000447102.8:c.702G= ENSP00000403536.2:p.Leu234=
ENST00000591788.3:c.254-37G=
ENST00000640164.1:n.403+132G=
ENST00000640762.1:c.501+132G= ENSP00000492031.1:n.501+132G=
ENST00000252288.6:c.570+132G= ENSP00000252288.1:n.570+132G=
ENST00000447102.7:c.702G= ENSP00000403536.2:p.Leu234=
ENST00000591788.2:c.256-37G= ENSP00000466341.2:n.256-37G=
NM_000156.5:c.570+132G= NP_000147.1:n.570+132G=
NM_138924.2:c.702G= NP_620279.1:p.Leu234=
NM_000156.6:c.570+132G= MANE Select NP_000147.1:n.570+132G=
NM_138924.3:c.702G= NP_620279.1:p.Leu234=