Canonical Allele Identifier: CA477367287

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898390A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027680A>C , CM000673.2:g.119027680A>C	GRCh38
NC_000011.9:g.118898390A>C , CM000673.1:g.118898390A>C	GRCh37
NC_000011.8:g.118403600A>C	NCBI36
NG_013331.1:g.8226T>G , LRG_187:g.8226T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.803T>G
ENST00000697845.1:n.727T>G
ENST00000697846.1:n.803T>G
ENST00000697847.1:n.803T>G
ENST00000697848.1:n.803T>G
ENST00000697849.1:n.1842T>G
ENST00000697850.1:n.803T>G
ENST00000697851.1:n.2163T>G
ENST00000638186.1:n.877T>G
ENST00000638360.1:n.709T>G
ENST00000638925.1:n.810T>G
ENST00000650539.1:n.979T>G
ENST00000330775.9:c.573T>G	ENSP00000476242.2:p.Pro191=
ENST00000357590.9:c.573T>G	ENSP00000476176.2:p.Pro191=
ENST00000524428.5:n.895T>G
ENST00000525039.5:n.997T>G
ENST00000525102.5:n.1331T>G
ENST00000525372.5:n.574T>G
ENST00000526275.5:n.1355T>G
ENST00000526626.6:n.536T>G
ENST00000527992.5:n.801T>G
ENST00000529510.5:n.399+514T>G
ENST00000530407.5:n.723T>G
ENST00000532085.1:n.3184T>G
ENST00000532888.6:n.869T>G
ENST00000538950.5:c.354T>G	ENSP00000475991.2:p.Pro118=
ENST00000545985.5:c.573T>G	ENSP00000475241.2:p.Pro191=
NM_001164277.1:c.573T>G , LRG_187t1:c.573T>G	NP_001157749.1:p.Pro191=
NM_001164278.1:c.573T>G	NP_001157750.1:p.Pro191=
NM_001164279.1:c.354T>G	NP_001157751.1:p.Pro118=
NM_001164280.1:c.573T>G	NP_001157752.1:p.Pro191=
NM_001467.5:c.573T>G	NP_001458.1:p.Pro191=
NM_001164278.2:c.573T>G	NP_001157750.1:p.Pro191=
NM_001164279.2:c.354T>G	NP_001157751.1:p.Pro118=
NM_001164280.2:c.573T>G	NP_001157752.1:p.Pro191=
NM_001467.6:c.573T>G	NP_001458.1:p.Pro191=
NM_001164277.2:c.573T>G MANE Select	NP_001157749.1:p.Pro191=