Canonical Allele Identifier: CA382899895

Gene: SLC37A4

Linked Data

• ClinVar Variation Id: 550983
• ClinVar RCV Id: RCV000665911
• dbSNP Id: rs1555190938
• MyVariant Identifiers: chr11:g.118897317G>A (hg19) ; chr11:g.119026607G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026607G>A , CM000673.2:g.119026607G>A	GRCh38
NC_000011.9:g.118897317G>A , CM000673.1:g.118897317G>A	GRCh37
NC_000011.8:g.118402527G>A	NCBI36
NG_013331.1:g.9299C>T , LRG_187:g.9299C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1014+330C>T
ENST00000697845.1:n.1268C>T
ENST00000697846.1:n.1014+330C>T
ENST00000697847.1:n.1096C>T
ENST00000697848.1:n.1096C>T
ENST00000697849.1:n.2383C>T
ENST00000697850.1:n.1096C>T
ENST00000697851.1:n.2704C>T
ENST00000638186.1:n.1170C>T
ENST00000638360.1:n.1002C>T
ENST00000638925.1:n.1103C>T
ENST00000650539.1:n.1272C>T
ENST00000330775.9:c.866C>T	ENSP00000476242.2:p.Ala289Val
ENST00000357590.9:c.866C>T	ENSP00000476176.2:p.Ala289Val
ENST00000524428.5:n.1106+330C>T
ENST00000525039.5:n.1290C>T
ENST00000525102.5:n.1624C>T
ENST00000525372.5:n.867C>T
ENST00000526275.5:n.1648C>T
ENST00000527992.5:n.1094C>T
ENST00000529510.5:n.558+330C>T
ENST00000530407.5:n.1016C>T
ENST00000532085.1:n.3725C>T
ENST00000538950.5:c.647C>T	ENSP00000475991.2:p.Ala216Val
ENST00000545985.5:c.866C>T	ENSP00000475241.2:p.Ala289Val
NM_001164277.1:c.866C>T , LRG_187t1:c.866C>T	NP_001157749.1:p.Ala289Val
NM_001164278.1:c.866C>T	NP_001157750.1:p.Ala289Val
NM_001164279.1:c.647C>T	NP_001157751.1:p.Ala216Val
NM_001164280.1:c.866C>T	NP_001157752.1:p.Ala289Val
NM_001467.5:c.866C>T	NP_001458.1:p.Ala289Val
NM_001164278.2:c.866C>T	NP_001157750.1:p.Ala289Val
NM_001164279.2:c.647C>T	NP_001157751.1:p.Ala216Val
NM_001164280.2:c.866C>T	NP_001157752.1:p.Ala289Val
NM_001467.6:c.866C>T	NP_001458.1:p.Ala289Val
NM_001164277.2:c.866C>T MANE Select	NP_001157749.1:p.Ala289Val