Canonical Allele Identifier: CA382897639

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118896727T>G (hg19) ; chr11:g.119026017T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026017T>G , CM000673.2:g.119026017T>G	GRCh38
NC_000011.9:g.118896727T>G , CM000673.1:g.118896727T>G	GRCh37
NC_000011.8:g.118401937T>G	NCBI36
NG_013331.1:g.9889A>C , LRG_187:g.9889A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1078A>C
ENST00000697845.1:n.1858A>C
ENST00000697846.1:n.1078A>C
ENST00000697847.1:n.1202-260A>C
ENST00000697848.1:n.1164A>C
ENST00000697849.1:n.2973A>C
ENST00000697850.1:n.1164A>C
ENST00000697851.1:n.2772A>C
ENST00000638186.1:n.1238A>C
ENST00000638360.1:n.1070A>C
ENST00000638925.1:n.1203A>C
ENST00000650539.1:n.1340A>C
ENST00000330775.9:c.934A>C	ENSP00000476242.2:p.Thr312Pro
ENST00000357590.9:c.934A>C	ENSP00000476176.2:p.Thr312Pro
ENST00000524428.5:n.1170A>C
ENST00000525039.5:n.1358A>C
ENST00000525102.5:n.1692A>C
ENST00000525372.5:n.1032A>C
ENST00000526275.5:n.1716A>C
ENST00000527992.5:n.1162A>C
ENST00000529510.5:n.622A>C
ENST00000530407.5:n.1084A>C
ENST00000532085.1:n.4315A>C
ENST00000538950.5:c.715A>C	ENSP00000475991.2:p.Thr239Pro
ENST00000545985.5:c.934A>C	ENSP00000475241.2:p.Thr312Pro
NM_001164277.1:c.934A>C , LRG_187t1:c.934A>C	NP_001157749.1:p.Thr312Pro
NM_001164278.1:c.934A>C	NP_001157750.1:p.Thr312Pro
NM_001164279.1:c.715A>C	NP_001157751.1:p.Thr239Pro
NM_001164280.1:c.934A>C	NP_001157752.1:p.Thr312Pro
NM_001467.5:c.934A>C	NP_001458.1:p.Thr312Pro
NM_001164278.2:c.934A>C	NP_001157750.1:p.Thr312Pro
NM_001164279.2:c.715A>C	NP_001157751.1:p.Thr239Pro
NM_001164280.2:c.934A>C	NP_001157752.1:p.Thr312Pro
NM_001467.6:c.934A>C	NP_001458.1:p.Thr312Pro
NM_001164277.2:c.934A>C MANE Select	NP_001157749.1:p.Thr312Pro