Canonical Allele Identifier: CA2003749319

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026976A= , CM000673.2:g.119026976A=	GRCh38
NC_000011.9:g.118897686A= , CM000673.1:g.118897686A=	GRCh37
NC_000011.8:g.118402896A=	NCBI36
NG_013331.1:g.8930T= , LRG_187:g.8930T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.975T=
ENST00000697845.1:n.899T=
ENST00000697846.1:n.975T=
ENST00000697847.1:n.975T=
ENST00000697848.1:n.975T=
ENST00000697849.1:n.2014T=
ENST00000697850.1:n.975T=
ENST00000697851.1:n.2335T=
ENST00000638186.1:n.1049T=
ENST00000638360.1:n.881T=
ENST00000638925.1:n.982T=
ENST00000650539.1:n.1151T=
ENST00000330775.9:c.745T=	ENSP00000476242.2:p.Phe249=
ENST00000357590.9:c.745T=	ENSP00000476176.2:p.Phe249=
ENST00000524428.5:n.1067T=
ENST00000525039.5:n.1169T=
ENST00000525102.5:n.1503T=
ENST00000525372.5:n.746T=
ENST00000526275.5:n.1527T=
ENST00000526626.6:n.708T=
ENST00000527992.5:n.973T=
ENST00000529510.5:n.519T=
ENST00000530407.5:n.895T=
ENST00000532085.1:n.3356T=
ENST00000532888.6:n.1041T=
ENST00000538950.5:c.526T=	ENSP00000475991.2:p.Phe176=
ENST00000545985.5:c.745T=	ENSP00000475241.2:p.Phe249=
NM_001164277.1:c.745T= , LRG_187t1:c.745T=	NP_001157749.1:p.Phe249=
NM_001164278.1:c.745T=	NP_001157750.1:p.Phe249=
NM_001164279.1:c.526T=	NP_001157751.1:p.Phe176=
NM_001164280.1:c.745T=	NP_001157752.1:p.Phe249=
NM_001467.5:c.745T=	NP_001458.1:p.Phe249=
NM_001164278.2:c.745T=	NP_001157750.1:p.Phe249=
NM_001164279.2:c.526T=	NP_001157751.1:p.Phe176=
NM_001164280.2:c.745T=	NP_001157752.1:p.Phe249=
NM_001467.6:c.745T=	NP_001458.1:p.Phe249=
NM_001164277.2:c.745T= MANE Select	NP_001157749.1:p.Phe249=