Canonical Allele Identifier: CA2003748852

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026041A= , CM000673.2:g.119026041A=	GRCh38
NC_000011.9:g.118896751A= , CM000673.1:g.118896751A=	GRCh37
NC_000011.8:g.118401961A=	NCBI36
NG_013331.1:g.9865T= , LRG_187:g.9865T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1054T=
ENST00000697845.1:n.1834T=
ENST00000697846.1:n.1054T=
ENST00000697847.1:n.1202-284T=
ENST00000697848.1:n.1140T=
ENST00000697849.1:n.2949T=
ENST00000697850.1:n.1140T=
ENST00000697851.1:n.2748T=
ENST00000638186.1:n.1214T=
ENST00000638360.1:n.1046T=
ENST00000638925.1:n.1179T=
ENST00000650539.1:n.1316T=
ENST00000330775.9:c.910T=	ENSP00000476242.2:p.Leu304=
ENST00000357590.9:c.910T=	ENSP00000476176.2:p.Leu304=
ENST00000524428.5:n.1146T=
ENST00000525039.5:n.1334T=
ENST00000525102.5:n.1668T=
ENST00000525372.5:n.1008T=
ENST00000526275.5:n.1692T=
ENST00000527992.5:n.1138T=
ENST00000529510.5:n.598T=
ENST00000530407.5:n.1060T=
ENST00000532085.1:n.4291T=
ENST00000538950.5:c.691T=	ENSP00000475991.2:p.Leu231=
ENST00000545985.5:c.910T=	ENSP00000475241.2:p.Leu304=
NM_001164277.1:c.910T= , LRG_187t1:c.910T=	NP_001157749.1:p.Leu304=
NM_001164278.1:c.910T=	NP_001157750.1:p.Leu304=
NM_001164279.1:c.691T=	NP_001157751.1:p.Leu231=
NM_001164280.1:c.910T=	NP_001157752.1:p.Leu304=
NM_001467.5:c.910T=	NP_001458.1:p.Leu304=
NM_001164278.2:c.910T=	NP_001157750.1:p.Leu304=
NM_001164279.2:c.691T=	NP_001157751.1:p.Leu231=
NM_001164280.2:c.910T=	NP_001157752.1:p.Leu304=
NM_001467.6:c.910T=	NP_001458.1:p.Leu304=
NM_001164277.2:c.910T= MANE Select	NP_001157749.1:p.Leu304=