Canonical Allele Identifier: CA2003749716

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027750C= , CM000673.2:g.119027750C=	GRCh38
NC_000011.9:g.118898460C= , CM000673.1:g.118898460C=	GRCh37
NC_000011.8:g.118403670C=	NCBI36
NG_013331.1:g.8157G= , LRG_187:g.8157G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.733G=
ENST00000697845.1:n.657G=
ENST00000697846.1:n.733G=
ENST00000697847.1:n.733G=
ENST00000697848.1:n.733G=
ENST00000697849.1:n.1772G=
ENST00000697850.1:n.733G=
ENST00000697851.1:n.2093G=
ENST00000638186.1:n.807G=
ENST00000638360.1:n.639G=
ENST00000638925.1:n.740G=
ENST00000650539.1:n.909G=
ENST00000330775.9:c.504G=	ENSP00000476242.2:p.Thr168=
ENST00000357590.9:c.504G=	ENSP00000476176.2:p.Thr168=
ENST00000524428.5:n.825G=
ENST00000525039.5:n.927G=
ENST00000525102.5:n.1261G=
ENST00000525372.5:n.504G=
ENST00000526275.5:n.1285G=
ENST00000526626.6:n.466G=
ENST00000527992.5:n.731G=
ENST00000529510.5:n.399+444G=
ENST00000530407.5:n.653G=
ENST00000532085.1:n.3114G=
ENST00000532888.6:n.799G=
ENST00000538950.5:c.285G=	ENSP00000475991.2:p.Thr95=
ENST00000545985.5:c.504G=	ENSP00000475241.2:p.Thr168=
NM_001164277.1:c.504G= , LRG_187t1:c.504G=	NP_001157749.1:p.Thr168=
NM_001164278.1:c.504G=	NP_001157750.1:p.Thr168=
NM_001164279.1:c.285G=	NP_001157751.1:p.Thr95=
NM_001164280.1:c.504G=	NP_001157752.1:p.Thr168=
NM_001467.5:c.504G=	NP_001458.1:p.Thr168=
NM_001164278.2:c.504G=	NP_001157750.1:p.Thr168=
NM_001164279.2:c.285G=	NP_001157751.1:p.Thr95=
NM_001164280.2:c.504G=	NP_001157752.1:p.Thr168=
NM_001467.6:c.504G=	NP_001458.1:p.Thr168=
NM_001164277.2:c.504G= MANE Select	NP_001157749.1:p.Thr168=