Canonical Allele Identifier: CA382901266

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897719C>T (hg19) ; chr11:g.119027009C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027009C>T , CM000673.2:g.119027009C>T	GRCh38
NC_000011.9:g.118897719C>T , CM000673.1:g.118897719C>T	GRCh37
NC_000011.8:g.118402929C>T	NCBI36
NG_013331.1:g.8897G>A , LRG_187:g.8897G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.942G>A
ENST00000697845.1:n.866G>A
ENST00000697846.1:n.942G>A
ENST00000697847.1:n.942G>A
ENST00000697848.1:n.942G>A
ENST00000697849.1:n.1981G>A
ENST00000697850.1:n.942G>A
ENST00000697851.1:n.2302G>A
ENST00000638186.1:n.1016G>A
ENST00000638360.1:n.848G>A
ENST00000638925.1:n.949G>A
ENST00000650539.1:n.1118G>A
ENST00000330775.9:c.712G>A	ENSP00000476242.2:p.Gly238Arg
ENST00000357590.9:c.712G>A	ENSP00000476176.2:p.Gly238Arg
ENST00000524428.5:n.1034G>A
ENST00000525039.5:n.1136G>A
ENST00000525102.5:n.1470G>A
ENST00000525372.5:n.713G>A
ENST00000526275.5:n.1494G>A
ENST00000526626.6:n.675G>A
ENST00000527992.5:n.940G>A
ENST00000529510.5:n.486G>A
ENST00000530407.5:n.862G>A
ENST00000532085.1:n.3323G>A
ENST00000532888.6:n.1008G>A
ENST00000538950.5:c.493G>A	ENSP00000475991.2:p.Gly165Arg
ENST00000545985.5:c.712G>A	ENSP00000475241.2:p.Gly238Arg
NM_001164277.1:c.712G>A , LRG_187t1:c.712G>A	NP_001157749.1:p.Gly238Arg
NM_001164278.1:c.712G>A	NP_001157750.1:p.Gly238Arg
NM_001164279.1:c.493G>A	NP_001157751.1:p.Gly165Arg
NM_001164280.1:c.712G>A	NP_001157752.1:p.Gly238Arg
NM_001467.5:c.712G>A	NP_001458.1:p.Gly238Arg
NM_001164278.2:c.712G>A	NP_001157750.1:p.Gly238Arg
NM_001164279.2:c.493G>A	NP_001157751.1:p.Gly165Arg
NM_001164280.2:c.712G>A	NP_001157752.1:p.Gly238Arg
NM_001467.6:c.712G>A	NP_001458.1:p.Gly238Arg
NM_001164277.2:c.712G>A MANE Select	NP_001157749.1:p.Gly238Arg