Canonical Allele Identifier: CA2003749136

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026632C= , CM000673.2:g.119026632C=	GRCh38
NC_000011.9:g.118897342C= , CM000673.1:g.118897342C=	GRCh37
NC_000011.8:g.118402552C=	NCBI36
NG_013331.1:g.9274G= , LRG_187:g.9274G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+305G=
ENST00000697845.1:n.1243G=
ENST00000697846.1:n.1014+305G=
ENST00000697847.1:n.1071G=
ENST00000697848.1:n.1071G=
ENST00000697849.1:n.2358G=
ENST00000697850.1:n.1071G=
ENST00000697851.1:n.2679G=
ENST00000638186.1:n.1145G=
ENST00000638360.1:n.977G=
ENST00000638925.1:n.1078G=
ENST00000650539.1:n.1247G=
ENST00000330775.9:c.841G=	ENSP00000476242.2:p.Gly281=
ENST00000357590.9:c.841G=	ENSP00000476176.2:p.Gly281=
ENST00000524428.5:n.1106+305G=
ENST00000525039.5:n.1265G=
ENST00000525102.5:n.1599G=
ENST00000525372.5:n.842G=
ENST00000526275.5:n.1623G=
ENST00000527992.5:n.1069G=
ENST00000529510.5:n.558+305G=
ENST00000530407.5:n.991G=
ENST00000532085.1:n.3700G=
ENST00000538950.5:c.622G=	ENSP00000475991.2:p.Gly208=
ENST00000545985.5:c.841G=	ENSP00000475241.2:p.Gly281=
NM_001164277.1:c.841G= , LRG_187t1:c.841G=	NP_001157749.1:p.Gly281=
NM_001164278.1:c.841G=	NP_001157750.1:p.Gly281=
NM_001164279.1:c.622G=	NP_001157751.1:p.Gly208=
NM_001164280.1:c.841G=	NP_001157752.1:p.Gly281=
NM_001467.5:c.841G=	NP_001458.1:p.Gly281=
NM_001164278.2:c.841G=	NP_001157750.1:p.Gly281=
NM_001164279.2:c.622G=	NP_001157751.1:p.Gly208=
NM_001164280.2:c.841G=	NP_001157752.1:p.Gly281=
NM_001467.6:c.841G=	NP_001458.1:p.Gly281=
NM_001164277.2:c.841G= MANE Select	NP_001157749.1:p.Gly281=