Canonical Allele Identifier: CA2573155789

Gene: GAMT

Linked Data

• ClinVar Variation Id: 1560222
• ClinVar RCV Id: RCV002195507
• dbSNP Id: rs900568054

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1399035G>C , CM000681.2:g.1399035G>C	GRCh38
NC_000019.9:g.1399034G>C , CM000681.1:g.1399034G>C	GRCh37
NC_000019.8:g.1350034G>C	NCBI36
NG_009785.1:g.7519C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252288.8:c.460-9C>G MANE Select	ENSP00000252288.1:n.460-9C>G
ENST00000447102.8:c.460-9C>G	ENSP00000403536.2:n.460-9C>G
ENST00000591788.3:c.143-9C>G
ENST00000640164.1:n.293-9C>G
ENST00000640762.1:c.391-9C>G	ENSP00000492031.1:n.391-9C>G
ENST00000252288.6:c.460-9C>G	ENSP00000252288.1:n.460-9C>G
ENST00000447102.7:c.460-9C>G	ENSP00000403536.2:n.460-9C>G
ENST00000591788.2:c.145-9C>G	ENSP00000466341.2:n.145-9C>G
NM_000156.5:c.460-9C>G	NP_000147.1:n.460-9C>G
NM_138924.2:c.460-9C>G	NP_620279.1:n.460-9C>G
NM_000156.6:c.460-9C>G MANE Select	NP_000147.1:n.460-9C>G
NM_138924.3:c.460-9C>G	NP_620279.1:n.460-9C>G