Canonical Allele Identifier: CA477125933

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897774C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027064C>T , CM000673.2:g.119027064C>T	GRCh38
NC_000011.9:g.118897774C>T , CM000673.1:g.118897774C>T	GRCh37
NC_000011.8:g.118402984C>T	NCBI36
NG_013331.1:g.8842G>A , LRG_187:g.8842G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.887G>A
ENST00000697845.1:n.811G>A
ENST00000697846.1:n.887G>A
ENST00000697847.1:n.887G>A
ENST00000697848.1:n.887G>A
ENST00000697849.1:n.1926G>A
ENST00000697850.1:n.887G>A
ENST00000697851.1:n.2247G>A
ENST00000638186.1:n.961G>A
ENST00000638360.1:n.793G>A
ENST00000638925.1:n.894G>A
ENST00000650539.1:n.1063G>A
ENST00000330775.9:c.657G>A	ENSP00000476242.2:p.Glu219=
ENST00000357590.9:c.657G>A	ENSP00000476176.2:p.Glu219=
ENST00000524428.5:n.979G>A
ENST00000525039.5:n.1081G>A
ENST00000525102.5:n.1415G>A
ENST00000525372.5:n.658G>A
ENST00000526275.5:n.1439G>A
ENST00000526626.6:n.620G>A
ENST00000527992.5:n.885G>A
ENST00000529510.5:n.431G>A
ENST00000530407.5:n.807G>A
ENST00000532085.1:n.3268G>A
ENST00000532888.6:n.953G>A
ENST00000538950.5:c.438G>A	ENSP00000475991.2:p.Glu146=
ENST00000545985.5:c.657G>A	ENSP00000475241.2:p.Glu219=
NM_001164277.1:c.657G>A , LRG_187t1:c.657G>A	NP_001157749.1:p.Glu219=
NM_001164278.1:c.657G>A	NP_001157750.1:p.Glu219=
NM_001164279.1:c.438G>A	NP_001157751.1:p.Glu146=
NM_001164280.1:c.657G>A	NP_001157752.1:p.Glu219=
NM_001467.5:c.657G>A	NP_001458.1:p.Glu219=
NM_001164278.2:c.657G>A	NP_001157750.1:p.Glu219=
NM_001164279.2:c.438G>A	NP_001157751.1:p.Glu146=
NM_001164280.2:c.657G>A	NP_001157752.1:p.Glu219=
NM_001467.6:c.657G>A	NP_001458.1:p.Glu219=
NM_001164277.2:c.657G>A MANE Select	NP_001157749.1:p.Glu219=