Canonical Allele Identifier: CA2003749643

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027639T= , CM000673.2:g.119027639T=	GRCh38
NC_000011.9:g.118898349T= , CM000673.1:g.118898349T=	GRCh37
NC_000011.8:g.118403559T=	NCBI36
NG_013331.1:g.8267A= , LRG_187:g.8267A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.844A=
ENST00000697845.1:n.768A=
ENST00000697846.1:n.844A=
ENST00000697847.1:n.844A=
ENST00000697848.1:n.844A=
ENST00000697849.1:n.1883A=
ENST00000697850.1:n.844A=
ENST00000697851.1:n.2204A=
ENST00000638186.1:n.918A=
ENST00000638360.1:n.750A=
ENST00000638925.1:n.851A=
ENST00000650539.1:n.1020A=
ENST00000330775.9:c.614A=	ENSP00000476242.2:p.Glu205=
ENST00000357590.9:c.614A=	ENSP00000476176.2:p.Glu205=
ENST00000524428.5:n.936A=
ENST00000525039.5:n.1038A=
ENST00000525102.5:n.1372A=
ENST00000525372.5:n.615A=
ENST00000526275.5:n.1396A=
ENST00000526626.6:n.577A=
ENST00000527992.5:n.842A=
ENST00000529510.5:n.400-544A=
ENST00000530407.5:n.764A=
ENST00000532085.1:n.3225A=
ENST00000532888.6:n.910A=
ENST00000538950.5:c.395A=	ENSP00000475991.2:p.Glu132=
ENST00000545985.5:c.614A=	ENSP00000475241.2:p.Glu205=
NM_001164277.1:c.614A= , LRG_187t1:c.614A=	NP_001157749.1:p.Glu205=
NM_001164278.1:c.614A=	NP_001157750.1:p.Glu205=
NM_001164279.1:c.395A=	NP_001157751.1:p.Glu132=
NM_001164280.1:c.614A=	NP_001157752.1:p.Glu205=
NM_001467.5:c.614A=	NP_001458.1:p.Glu205=
NM_001164278.2:c.614A=	NP_001157750.1:p.Glu205=
NM_001164279.2:c.395A=	NP_001157751.1:p.Glu132=
NM_001164280.2:c.614A=	NP_001157752.1:p.Glu205=
NM_001467.6:c.614A=	NP_001458.1:p.Glu205=
NM_001164277.2:c.614A= MANE Select	NP_001157749.1:p.Glu205=