Canonical Allele Identifier: CA477367907

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898571T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027861T>G , CM000673.2:g.119027861T>G	GRCh38
NC_000011.9:g.118898571T>G , CM000673.1:g.118898571T>G	GRCh37
NC_000011.8:g.118403781T>G	NCBI36
NG_013331.1:g.8046A>C , LRG_187:g.8046A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.622A>C
ENST00000697845.1:n.546A>C
ENST00000697846.1:n.622A>C
ENST00000697847.1:n.622A>C
ENST00000697848.1:n.622A>C
ENST00000697849.1:n.1661A>C
ENST00000697850.1:n.622A>C
ENST00000697851.1:n.1982A>C
ENST00000638186.1:n.696A>C
ENST00000638360.1:n.619-91A>C
ENST00000638925.1:n.629A>C
ENST00000650539.1:n.798A>C
ENST00000330775.9:c.393A>C	ENSP00000476242.2:p.Pro131=
ENST00000357590.9:c.393A>C	ENSP00000476176.2:p.Pro131=
ENST00000524428.5:n.714A>C
ENST00000525039.5:n.816A>C
ENST00000525102.5:n.1150A>C
ENST00000525372.5:n.393A>C
ENST00000525787.1:n.1009A>C
ENST00000526275.5:n.1174A>C
ENST00000526626.6:n.355A>C
ENST00000527992.5:n.620A>C
ENST00000529510.5:n.399+333A>C
ENST00000530407.5:n.542A>C
ENST00000532085.1:n.3003A>C
ENST00000532888.6:n.688A>C
ENST00000538950.5:c.174A>C	ENSP00000475991.2:p.Pro58=
ENST00000545985.5:c.393A>C	ENSP00000475241.2:p.Pro131=
NM_001164277.1:c.393A>C , LRG_187t1:c.393A>C	NP_001157749.1:p.Pro131=
NM_001164278.1:c.393A>C	NP_001157750.1:p.Pro131=
NM_001164279.1:c.174A>C	NP_001157751.1:p.Pro58=
NM_001164280.1:c.393A>C	NP_001157752.1:p.Pro131=
NM_001467.5:c.393A>C	NP_001458.1:p.Pro131=
NM_001164278.2:c.393A>C	NP_001157750.1:p.Pro131=
NM_001164279.2:c.174A>C	NP_001157751.1:p.Pro58=
NM_001164280.2:c.393A>C	NP_001157752.1:p.Pro131=
NM_001467.6:c.393A>C	NP_001458.1:p.Pro131=
NM_001164277.2:c.393A>C MANE Select	NP_001157749.1:p.Pro131=