Canonical Allele Identifier: CA2003749310

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026961C= , CM000673.2:g.119026961C=	GRCh38
NC_000011.9:g.118897671C= , CM000673.1:g.118897671C=	GRCh37
NC_000011.8:g.118402881C=	NCBI36
NG_013331.1:g.8945G= , LRG_187:g.8945G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.990G=
ENST00000697845.1:n.914G=
ENST00000697846.1:n.990G=
ENST00000697847.1:n.990G=
ENST00000697848.1:n.990G=
ENST00000697849.1:n.2029G=
ENST00000697850.1:n.990G=
ENST00000697851.1:n.2350G=
ENST00000638186.1:n.1064G=
ENST00000638360.1:n.896G=
ENST00000638925.1:n.997G=
ENST00000650539.1:n.1166G=
ENST00000330775.9:c.760G=	ENSP00000476242.2:p.Glu254=
ENST00000357590.9:c.760G=	ENSP00000476176.2:p.Glu254=
ENST00000524428.5:n.1082G=
ENST00000525039.5:n.1184G=
ENST00000525102.5:n.1518G=
ENST00000525372.5:n.761G=
ENST00000526275.5:n.1542G=
ENST00000526626.6:n.723G=
ENST00000527992.5:n.988G=
ENST00000529510.5:n.534G=
ENST00000530407.5:n.910G=
ENST00000532085.1:n.3371G=
ENST00000532888.6:n.1056G=
ENST00000538950.5:c.541G=	ENSP00000475991.2:p.Glu181=
ENST00000545985.5:c.760G=	ENSP00000475241.2:p.Glu254=
NM_001164277.1:c.760G= , LRG_187t1:c.760G=	NP_001157749.1:p.Glu254=
NM_001164278.1:c.760G=	NP_001157750.1:p.Glu254=
NM_001164279.1:c.541G=	NP_001157751.1:p.Glu181=
NM_001164280.1:c.760G=	NP_001157752.1:p.Glu254=
NM_001467.5:c.760G=	NP_001458.1:p.Glu254=
NM_001164278.2:c.760G=	NP_001157750.1:p.Glu254=
NM_001164279.2:c.541G=	NP_001157751.1:p.Glu181=
NM_001164280.2:c.760G=	NP_001157752.1:p.Glu254=
NM_001467.6:c.760G=	NP_001458.1:p.Glu254=
NM_001164277.2:c.760G= MANE Select	NP_001157749.1:p.Glu254=