Canonical Allele Identifier: CA382907962

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118899939A>T (hg19) ; chr11:g.119029229A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029229A>T , CM000673.2:g.119029229A>T	GRCh38
NC_000011.9:g.118899939A>T , CM000673.1:g.118899939A>T	GRCh37
NC_000011.8:g.118405149A>T	NCBI36
NG_013331.1:g.6678T>A , LRG_187:g.6678T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.370T>A
ENST00000697846.1:n.370T>A
ENST00000697847.1:n.370T>A
ENST00000697848.1:n.370T>A
ENST00000697849.1:n.614T>A
ENST00000697850.1:n.370T>A
ENST00000697851.1:n.614T>A
ENST00000638186.1:n.444T>A
ENST00000638360.1:n.378T>A
ENST00000638925.1:n.377T>A
ENST00000650539.1:n.546T>A
ENST00000330775.9:c.141T>A	ENSP00000476242.2:p.Asp47Glu
ENST00000357590.9:c.141T>A	ENSP00000476176.2:p.Asp47Glu
ENST00000524428.5:n.141T>A
ENST00000525039.5:n.564T>A
ENST00000525102.5:n.898T>A
ENST00000525372.5:n.141T>A
ENST00000525787.1:n.436T>A
ENST00000526626.6:n.336T>A
ENST00000527992.5:n.368T>A
ENST00000529510.5:n.159T>A
ENST00000530407.5:n.197+163T>A
ENST00000532085.1:n.1635T>A
ENST00000532888.6:n.336T>A
ENST00000534384.1:n.361T>A
ENST00000538950.5:c.-172+163T>A	ENSP00000475991.2:n.-172+163T>A
ENST00000545985.5:c.141T>A	ENSP00000475241.2:p.Asp47Glu
NM_001164277.1:c.141T>A , LRG_187t1:c.141T>A	NP_001157749.1:p.Asp47Glu
NM_001164278.1:c.141T>A	NP_001157750.1:p.Asp47Glu
NM_001164279.1:c.-172+163T>A	NP_001157751.1:n.-172+163T>A
NM_001164280.1:c.141T>A	NP_001157752.1:p.Asp47Glu
NM_001467.5:c.141T>A	NP_001458.1:p.Asp47Glu
NM_001164278.2:c.141T>A	NP_001157750.1:p.Asp47Glu
NM_001164279.2:c.-172+163T>A	NP_001157751.1:n.-172+163T>A
NM_001164280.2:c.141T>A	NP_001157752.1:p.Asp47Glu
NM_001467.6:c.141T>A	NP_001458.1:p.Asp47Glu
NM_001164277.2:c.141T>A MANE Select	NP_001157749.1:p.Asp47Glu