Canonical Allele Identifier: CA477125359

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026666-C-A
• MyVariant Identifiers: chr11:g.118897376C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026666C>A , CM000673.2:g.119026666C>A	GRCh38
NC_000011.9:g.118897376C>A , CM000673.1:g.118897376C>A	GRCh37
NC_000011.8:g.118402586C>A	NCBI36
NG_013331.1:g.9240G>T , LRG_187:g.9240G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+271G>T
ENST00000697845.1:n.1209G>T
ENST00000697846.1:n.1014+271G>T
ENST00000697847.1:n.1037G>T
ENST00000697848.1:n.1037G>T
ENST00000697849.1:n.2324G>T
ENST00000697850.1:n.1037G>T
ENST00000697851.1:n.2645G>T
ENST00000638186.1:n.1111G>T
ENST00000638360.1:n.943G>T
ENST00000638925.1:n.1044G>T
ENST00000650539.1:n.1213G>T
ENST00000330775.9:c.807G>T	ENSP00000476242.2:p.Leu269=
ENST00000357590.9:c.807G>T	ENSP00000476176.2:p.Leu269=
ENST00000524428.5:n.1106+271G>T
ENST00000525039.5:n.1231G>T
ENST00000525102.5:n.1565G>T
ENST00000525372.5:n.808G>T
ENST00000526275.5:n.1589G>T
ENST00000527992.5:n.1035G>T
ENST00000529510.5:n.558+271G>T
ENST00000530407.5:n.957G>T
ENST00000532085.1:n.3666G>T
ENST00000532888.6:n.1351G>T
ENST00000538950.5:c.588G>T	ENSP00000475991.2:p.Leu196=
ENST00000545985.5:c.807G>T	ENSP00000475241.2:p.Leu269=
NM_001164277.1:c.807G>T , LRG_187t1:c.807G>T	NP_001157749.1:p.Leu269=
NM_001164278.1:c.807G>T	NP_001157750.1:p.Leu269=
NM_001164279.1:c.588G>T	NP_001157751.1:p.Leu196=
NM_001164280.1:c.807G>T	NP_001157752.1:p.Leu269=
NM_001467.5:c.807G>T	NP_001458.1:p.Leu269=
NM_001164278.2:c.807G>T	NP_001157750.1:p.Leu269=
NM_001164279.2:c.588G>T	NP_001157751.1:p.Leu196=
NM_001164280.2:c.807G>T	NP_001157752.1:p.Leu269=
NM_001467.6:c.807G>T	NP_001458.1:p.Leu269=
NM_001164277.2:c.807G>T MANE Select	NP_001157749.1:p.Leu269=