Canonical Allele Identifier: CA2003749356

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027051G= , CM000673.2:g.119027051G=	GRCh38
NC_000011.9:g.118897761G= , CM000673.1:g.118897761G=	GRCh37
NC_000011.8:g.118402971G=	NCBI36
NG_013331.1:g.8855C= , LRG_187:g.8855C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.900C=
ENST00000697845.1:n.824C=
ENST00000697846.1:n.900C=
ENST00000697847.1:n.900C=
ENST00000697848.1:n.900C=
ENST00000697849.1:n.1939C=
ENST00000697850.1:n.900C=
ENST00000697851.1:n.2260C=
ENST00000638186.1:n.974C=
ENST00000638360.1:n.806C=
ENST00000638925.1:n.907C=
ENST00000650539.1:n.1076C=
ENST00000330775.9:c.670C=	ENSP00000476242.2:p.Pro224=
ENST00000357590.9:c.670C=	ENSP00000476176.2:p.Pro224=
ENST00000524428.5:n.992C=
ENST00000525039.5:n.1094C=
ENST00000525102.5:n.1428C=
ENST00000525372.5:n.671C=
ENST00000526275.5:n.1452C=
ENST00000526626.6:n.633C=
ENST00000527992.5:n.898C=
ENST00000529510.5:n.444C=
ENST00000530407.5:n.820C=
ENST00000532085.1:n.3281C=
ENST00000532888.6:n.966C=
ENST00000538950.5:c.451C=	ENSP00000475991.2:p.Pro151=
ENST00000545985.5:c.670C=	ENSP00000475241.2:p.Pro224=
NM_001164277.1:c.670C= , LRG_187t1:c.670C=	NP_001157749.1:p.Pro224=
NM_001164278.1:c.670C=	NP_001157750.1:p.Pro224=
NM_001164279.1:c.451C=	NP_001157751.1:p.Pro151=
NM_001164280.1:c.670C=	NP_001157752.1:p.Pro224=
NM_001467.5:c.670C=	NP_001458.1:p.Pro224=
NM_001164278.2:c.670C=	NP_001157750.1:p.Pro224=
NM_001164279.2:c.451C=	NP_001157751.1:p.Pro151=
NM_001164280.2:c.670C=	NP_001157752.1:p.Pro224=
NM_001467.6:c.670C=	NP_001458.1:p.Pro224=
NM_001164277.2:c.670C= MANE Select	NP_001157749.1:p.Pro224=