Canonical Allele Identifier: CA2003749331

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026998G= , CM000673.2:g.119026998G=	GRCh38
NC_000011.9:g.118897708G= , CM000673.1:g.118897708G=	GRCh37
NC_000011.8:g.118402918G=	NCBI36
NG_013331.1:g.8908C= , LRG_187:g.8908C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.953C=
ENST00000697845.1:n.877C=
ENST00000697846.1:n.953C=
ENST00000697847.1:n.953C=
ENST00000697848.1:n.953C=
ENST00000697849.1:n.1992C=
ENST00000697850.1:n.953C=
ENST00000697851.1:n.2313C=
ENST00000638186.1:n.1027C=
ENST00000638360.1:n.859C=
ENST00000638925.1:n.960C=
ENST00000650539.1:n.1129C=
ENST00000330775.9:c.723C=	ENSP00000476242.2:p.Thr241=
ENST00000357590.9:c.723C=	ENSP00000476176.2:p.Thr241=
ENST00000524428.5:n.1045C=
ENST00000525039.5:n.1147C=
ENST00000525102.5:n.1481C=
ENST00000525372.5:n.724C=
ENST00000526275.5:n.1505C=
ENST00000526626.6:n.686C=
ENST00000527992.5:n.951C=
ENST00000529510.5:n.497C=
ENST00000530407.5:n.873C=
ENST00000532085.1:n.3334C=
ENST00000532888.6:n.1019C=
ENST00000538950.5:c.504C=	ENSP00000475991.2:p.Thr168=
ENST00000545985.5:c.723C=	ENSP00000475241.2:p.Thr241=
NM_001164277.1:c.723C= , LRG_187t1:c.723C=	NP_001157749.1:p.Thr241=
NM_001164278.1:c.723C=	NP_001157750.1:p.Thr241=
NM_001164279.1:c.504C=	NP_001157751.1:p.Thr168=
NM_001164280.1:c.723C=	NP_001157752.1:p.Thr241=
NM_001467.5:c.723C=	NP_001458.1:p.Thr241=
NM_001164278.2:c.723C=	NP_001157750.1:p.Thr241=
NM_001164279.2:c.504C=	NP_001157751.1:p.Thr168=
NM_001164280.2:c.723C=	NP_001157752.1:p.Thr241=
NM_001467.6:c.723C=	NP_001458.1:p.Thr241=
NM_001164277.2:c.723C= MANE Select	NP_001157749.1:p.Thr241=