Canonical Allele Identifier: CA2003775414

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1943682596

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029418C>T , CM000673.2:g.119029418C>T	GRCh38
NC_000011.9:g.118900128C>T , CM000673.1:g.118900128C>T	GRCh37
NC_000011.8:g.118405338C>T	NCBI36
NG_013331.1:g.6489G>A , LRG_187:g.6489G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.181G>A
ENST00000697846.1:n.181G>A
ENST00000697847.1:n.181G>A
ENST00000697848.1:n.181G>A
ENST00000697849.1:n.425G>A
ENST00000697850.1:n.181G>A
ENST00000697851.1:n.425G>A
ENST00000638186.1:n.255G>A
ENST00000638360.1:n.189G>A
ENST00000638925.1:n.188G>A
ENST00000650539.1:n.357G>A
ENST00000330775.9:c.-49G>A	ENSP00000476242.2:n.-49G>A
ENST00000357590.9:c.-49G>A	ENSP00000476176.2:n.-49G>A
ENST00000525039.5:n.375G>A
ENST00000525102.5:n.709G>A
ENST00000525787.1:n.247G>A
ENST00000526626.6:n.147G>A
ENST00000527992.5:n.179G>A
ENST00000530407.5:n.171G>A
ENST00000532085.1:n.1446G>A
ENST00000532888.6:n.147G>A
ENST00000534384.1:n.172G>A
ENST00000538950.5:c.-198G>A	ENSP00000475991.2:n.-198G>A
ENST00000545985.5:c.-49G>A	ENSP00000475241.2:n.-49G>A
NM_001164277.1:c.-49G>A , LRG_187t1:c.-49G>A	NP_001157749.1:n.-49G>A
NM_001164278.1:c.-49G>A	NP_001157750.1:n.-49G>A
NM_001164279.1:c.-198G>A	NP_001157751.1:n.-198G>A
NM_001164280.1:c.-49G>A	NP_001157752.1:n.-49G>A
NM_001467.5:c.-49G>A	NP_001458.1:n.-49G>A
NM_001164278.2:c.-49G>A	NP_001157750.1:n.-49G>A
NM_001164279.2:c.-198G>A	NP_001157751.1:n.-198G>A
NM_001164280.2:c.-49G>A	NP_001157752.1:n.-49G>A
NM_001467.6:c.-49G>A	NP_001458.1:n.-49G>A
NM_001164277.2:c.-49G>A MANE Select	NP_001157749.1:n.-49G>A