Canonical Allele Identifier: CA477367902

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1555191386
• MyVariant Identifiers: chr11:g.118898562A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027852A>G , CM000673.2:g.119027852A>G	GRCh38
NC_000011.9:g.118898562A>G , CM000673.1:g.118898562A>G	GRCh37
NC_000011.8:g.118403772A>G	NCBI36
NG_013331.1:g.8055T>C , LRG_187:g.8055T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.631T>C
ENST00000697845.1:n.555T>C
ENST00000697846.1:n.631T>C
ENST00000697847.1:n.631T>C
ENST00000697848.1:n.631T>C
ENST00000697849.1:n.1670T>C
ENST00000697850.1:n.631T>C
ENST00000697851.1:n.1991T>C
ENST00000638186.1:n.705T>C
ENST00000638360.1:n.619-82T>C
ENST00000638925.1:n.638T>C
ENST00000650539.1:n.807T>C
ENST00000330775.9:c.402T>C	ENSP00000476242.2:p.Phe134=
ENST00000357590.9:c.402T>C	ENSP00000476176.2:p.Phe134=
ENST00000524428.5:n.723T>C
ENST00000525039.5:n.825T>C
ENST00000525102.5:n.1159T>C
ENST00000525372.5:n.402T>C
ENST00000525787.1:n.1018T>C
ENST00000526275.5:n.1183T>C
ENST00000526626.6:n.364T>C
ENST00000527992.5:n.629T>C
ENST00000529510.5:n.399+342T>C
ENST00000530407.5:n.551T>C
ENST00000532085.1:n.3012T>C
ENST00000532888.6:n.697T>C
ENST00000538950.5:c.183T>C	ENSP00000475991.2:p.Phe61=
ENST00000545985.5:c.402T>C	ENSP00000475241.2:p.Phe134=
NM_001164277.1:c.402T>C , LRG_187t1:c.402T>C	NP_001157749.1:p.Phe134=
NM_001164278.1:c.402T>C	NP_001157750.1:p.Phe134=
NM_001164279.1:c.183T>C	NP_001157751.1:p.Phe61=
NM_001164280.1:c.402T>C	NP_001157752.1:p.Phe134=
NM_001467.5:c.402T>C	NP_001458.1:p.Phe134=
NM_001164278.2:c.402T>C	NP_001157750.1:p.Phe134=
NM_001164279.2:c.183T>C	NP_001157751.1:p.Phe61=
NM_001164280.2:c.402T>C	NP_001157752.1:p.Phe134=
NM_001467.6:c.402T>C	NP_001458.1:p.Phe134=
NM_001164277.2:c.402T>C MANE Select	NP_001157749.1:p.Phe134=