Canonical Allele Identifier: CA2003749721

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027759C= , CM000673.2:g.119027759C=	GRCh38
NC_000011.9:g.118898469C= , CM000673.1:g.118898469C=	GRCh37
NC_000011.8:g.118403679C=	NCBI36
NG_013331.1:g.8148G= , LRG_187:g.8148G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.724G=
ENST00000697845.1:n.648G=
ENST00000697846.1:n.724G=
ENST00000697847.1:n.724G=
ENST00000697848.1:n.724G=
ENST00000697849.1:n.1763G=
ENST00000697850.1:n.724G=
ENST00000697851.1:n.2084G=
ENST00000638186.1:n.798G=
ENST00000638360.1:n.630G=
ENST00000638925.1:n.731G=
ENST00000650539.1:n.900G=
ENST00000330775.9:c.495G=	ENSP00000476242.2:p.Trp165=
ENST00000357590.9:c.495G=	ENSP00000476176.2:p.Trp165=
ENST00000524428.5:n.816G=
ENST00000525039.5:n.918G=
ENST00000525102.5:n.1252G=
ENST00000525372.5:n.495G=
ENST00000526275.5:n.1276G=
ENST00000526626.6:n.457G=
ENST00000527992.5:n.722G=
ENST00000529510.5:n.399+435G=
ENST00000530407.5:n.644G=
ENST00000532085.1:n.3105G=
ENST00000532888.6:n.790G=
ENST00000538950.5:c.276G=	ENSP00000475991.2:p.Trp92=
ENST00000545985.5:c.495G=	ENSP00000475241.2:p.Trp165=
NM_001164277.1:c.495G= , LRG_187t1:c.495G=	NP_001157749.1:p.Trp165=
NM_001164278.1:c.495G=	NP_001157750.1:p.Trp165=
NM_001164279.1:c.276G=	NP_001157751.1:p.Trp92=
NM_001164280.1:c.495G=	NP_001157752.1:p.Trp165=
NM_001467.5:c.495G=	NP_001458.1:p.Trp165=
NM_001164278.2:c.495G=	NP_001157750.1:p.Trp165=
NM_001164279.2:c.276G=	NP_001157751.1:p.Trp92=
NM_001164280.2:c.495G=	NP_001157752.1:p.Trp165=
NM_001467.6:c.495G=	NP_001458.1:p.Trp165=
NM_001164277.2:c.495G= MANE Select	NP_001157749.1:p.Trp165=