Canonical Allele Identifier: CA2317699417

Gene: GAMT

Linked Data

• dbSNP Id: rs2082621979
• gnomAD v4: 19-1399683-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1399683G>C , CM000681.2:g.1399683G>C	GRCh38
NC_000019.9:g.1399682G>C , CM000681.1:g.1399682G>C	GRCh37
NC_000019.8:g.1350682G>C	NCBI36
NG_009785.1:g.6871C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252288.8:c.328-96C>G MANE Select	ENSP00000252288.1:n.328-96C>G
ENST00000447102.8:c.328-96C>G	ENSP00000403536.2:n.328-96C>G
ENST00000591788.3:c.11-96C>G
ENST00000640164.1:n.65C>G
ENST00000640762.1:c.259-96C>G	ENSP00000492031.1:n.259-96C>G
ENST00000252288.6:c.328-96C>G	ENSP00000252288.1:n.328-96C>G
ENST00000447102.7:c.328-96C>G	ENSP00000403536.2:n.328-96C>G
ENST00000591788.2:c.13-96C>G	ENSP00000466341.2:n.13-96C>G
NM_000156.5:c.328-96C>G	NP_000147.1:n.328-96C>G
NM_138924.2:c.328-96C>G	NP_620279.1:n.328-96C>G
NM_000156.6:c.328-96C>G MANE Select	NP_000147.1:n.328-96C>G
NM_138924.3:c.328-96C>G	NP_620279.1:n.328-96C>G