Canonical Allele Identifier: CA2003749750

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027811G= , CM000673.2:g.119027811G=	GRCh38
NC_000011.9:g.118898521G= , CM000673.1:g.118898521G=	GRCh37
NC_000011.8:g.118403731G=	NCBI36
NG_013331.1:g.8096C= , LRG_187:g.8096C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.672C=
ENST00000697845.1:n.596C=
ENST00000697846.1:n.672C=
ENST00000697847.1:n.672C=
ENST00000697848.1:n.672C=
ENST00000697849.1:n.1711C=
ENST00000697850.1:n.672C=
ENST00000697851.1:n.2032C=
ENST00000638186.1:n.746C=
ENST00000638360.1:n.619-41C=
ENST00000638925.1:n.679C=
ENST00000650539.1:n.848C=
ENST00000330775.9:c.443C=	ENSP00000476242.2:p.Ala148=
ENST00000357590.9:c.443C=	ENSP00000476176.2:p.Ala148=
ENST00000524428.5:n.764C=
ENST00000525039.5:n.866C=
ENST00000525102.5:n.1200C=
ENST00000525372.5:n.443C=
ENST00000526275.5:n.1224C=
ENST00000526626.6:n.405C=
ENST00000527992.5:n.670C=
ENST00000529510.5:n.399+383C=
ENST00000530407.5:n.592C=
ENST00000532085.1:n.3053C=
ENST00000532888.6:n.738C=
ENST00000538950.5:c.224C=	ENSP00000475991.2:p.Ala75=
ENST00000545985.5:c.443C=	ENSP00000475241.2:p.Ala148=
NM_001164277.1:c.443C= , LRG_187t1:c.443C=	NP_001157749.1:p.Ala148=
NM_001164278.1:c.443C=	NP_001157750.1:p.Ala148=
NM_001164279.1:c.224C=	NP_001157751.1:p.Ala75=
NM_001164280.1:c.443C=	NP_001157752.1:p.Ala148=
NM_001467.5:c.443C=	NP_001458.1:p.Ala148=
NM_001164278.2:c.443C=	NP_001157750.1:p.Ala148=
NM_001164279.2:c.224C=	NP_001157751.1:p.Ala75=
NM_001164280.2:c.443C=	NP_001157752.1:p.Ala148=
NM_001467.6:c.443C=	NP_001458.1:p.Ala148=
NM_001164277.2:c.443C= MANE Select	NP_001157749.1:p.Ala148=