Canonical Allele Identifier: CA2003749646

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027644G= , CM000673.2:g.119027644G=	GRCh38
NC_000011.9:g.118898354G= , CM000673.1:g.118898354G=	GRCh37
NC_000011.8:g.118403564G=	NCBI36
NG_013331.1:g.8262C= , LRG_187:g.8262C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.839C=
ENST00000697845.1:n.763C=
ENST00000697846.1:n.839C=
ENST00000697847.1:n.839C=
ENST00000697848.1:n.839C=
ENST00000697849.1:n.1878C=
ENST00000697850.1:n.839C=
ENST00000697851.1:n.2199C=
ENST00000638186.1:n.913C=
ENST00000638360.1:n.745C=
ENST00000638925.1:n.846C=
ENST00000650539.1:n.1015C=
ENST00000330775.9:c.609C=	ENSP00000476242.2:p.Pro203=
ENST00000357590.9:c.609C=	ENSP00000476176.2:p.Pro203=
ENST00000524428.5:n.931C=
ENST00000525039.5:n.1033C=
ENST00000525102.5:n.1367C=
ENST00000525372.5:n.610C=
ENST00000526275.5:n.1391C=
ENST00000526626.6:n.572C=
ENST00000527992.5:n.837C=
ENST00000529510.5:n.400-549C=
ENST00000530407.5:n.759C=
ENST00000532085.1:n.3220C=
ENST00000532888.6:n.905C=
ENST00000538950.5:c.390C=	ENSP00000475991.2:p.Pro130=
ENST00000545985.5:c.609C=	ENSP00000475241.2:p.Pro203=
NM_001164277.1:c.609C= , LRG_187t1:c.609C=	NP_001157749.1:p.Pro203=
NM_001164278.1:c.609C=	NP_001157750.1:p.Pro203=
NM_001164279.1:c.390C=	NP_001157751.1:p.Pro130=
NM_001164280.1:c.609C=	NP_001157752.1:p.Pro203=
NM_001467.5:c.609C=	NP_001458.1:p.Pro203=
NM_001164278.2:c.609C=	NP_001157750.1:p.Pro203=
NM_001164279.2:c.390C=	NP_001157751.1:p.Pro130=
NM_001164280.2:c.609C=	NP_001157752.1:p.Pro203=
NM_001467.6:c.609C=	NP_001458.1:p.Pro203=
NM_001164277.2:c.609C= MANE Select	NP_001157749.1:p.Pro203=