Canonical Allele Identifier: CA382901117

Gene: SLC37A4

Linked Data

• dbSNP Id: rs2134634891
• MyVariant Identifiers: chr11:g.118897697T>G (hg19) ; chr11:g.119026987T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026987T>G , CM000673.2:g.119026987T>G	GRCh38
NC_000011.9:g.118897697T>G , CM000673.1:g.118897697T>G	GRCh37
NC_000011.8:g.118402907T>G	NCBI36
NG_013331.1:g.8919A>C , LRG_187:g.8919A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.964A>C
ENST00000697845.1:n.888A>C
ENST00000697846.1:n.964A>C
ENST00000697847.1:n.964A>C
ENST00000697848.1:n.964A>C
ENST00000697849.1:n.2003A>C
ENST00000697850.1:n.964A>C
ENST00000697851.1:n.2324A>C
ENST00000638186.1:n.1038A>C
ENST00000638360.1:n.870A>C
ENST00000638925.1:n.971A>C
ENST00000650539.1:n.1140A>C
ENST00000330775.9:c.734A>C	ENSP00000476242.2:p.Asp245Ala
ENST00000357590.9:c.734A>C	ENSP00000476176.2:p.Asp245Ala
ENST00000524428.5:n.1056A>C
ENST00000525039.5:n.1158A>C
ENST00000525102.5:n.1492A>C
ENST00000525372.5:n.735A>C
ENST00000526275.5:n.1516A>C
ENST00000526626.6:n.697A>C
ENST00000527992.5:n.962A>C
ENST00000529510.5:n.508A>C
ENST00000530407.5:n.884A>C
ENST00000532085.1:n.3345A>C
ENST00000532888.6:n.1030A>C
ENST00000538950.5:c.515A>C	ENSP00000475991.2:p.Asp172Ala
ENST00000545985.5:c.734A>C	ENSP00000475241.2:p.Asp245Ala
NM_001164277.1:c.734A>C , LRG_187t1:c.734A>C	NP_001157749.1:p.Asp245Ala
NM_001164278.1:c.734A>C	NP_001157750.1:p.Asp245Ala
NM_001164279.1:c.515A>C	NP_001157751.1:p.Asp172Ala
NM_001164280.1:c.734A>C	NP_001157752.1:p.Asp245Ala
NM_001467.5:c.734A>C	NP_001458.1:p.Asp245Ala
NM_001164278.2:c.734A>C	NP_001157750.1:p.Asp245Ala
NM_001164279.2:c.515A>C	NP_001157751.1:p.Asp172Ala
NM_001164280.2:c.734A>C	NP_001157752.1:p.Asp245Ala
NM_001467.6:c.734A>C	NP_001458.1:p.Asp245Ala
NM_001164277.2:c.734A>C MANE Select	NP_001157749.1:p.Asp245Ala