Canonical Allele Identifier: CA2003749148

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026653G= , CM000673.2:g.119026653G=	GRCh38
NC_000011.9:g.118897363G= , CM000673.1:g.118897363G=	GRCh37
NC_000011.8:g.118402573G=	NCBI36
NG_013331.1:g.9253C= , LRG_187:g.9253C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1014+284C=
ENST00000697845.1:n.1222C=
ENST00000697846.1:n.1014+284C=
ENST00000697847.1:n.1050C=
ENST00000697848.1:n.1050C=
ENST00000697849.1:n.2337C=
ENST00000697850.1:n.1050C=
ENST00000697851.1:n.2658C=
ENST00000638186.1:n.1124C=
ENST00000638360.1:n.956C=
ENST00000638925.1:n.1057C=
ENST00000650539.1:n.1226C=
ENST00000330775.9:c.820C=	ENSP00000476242.2:p.Leu274=
ENST00000357590.9:c.820C=	ENSP00000476176.2:p.Leu274=
ENST00000524428.5:n.1106+284C=
ENST00000525039.5:n.1244C=
ENST00000525102.5:n.1578C=
ENST00000525372.5:n.821C=
ENST00000526275.5:n.1602C=
ENST00000527992.5:n.1048C=
ENST00000529510.5:n.558+284C=
ENST00000530407.5:n.970C=
ENST00000532085.1:n.3679C=
ENST00000538950.5:c.601C=	ENSP00000475991.2:p.Leu201=
ENST00000545985.5:c.820C=	ENSP00000475241.2:p.Leu274=
NM_001164277.1:c.820C= , LRG_187t1:c.820C=	NP_001157749.1:p.Leu274=
NM_001164278.1:c.820C=	NP_001157750.1:p.Leu274=
NM_001164279.1:c.601C=	NP_001157751.1:p.Leu201=
NM_001164280.1:c.820C=	NP_001157752.1:p.Leu274=
NM_001467.5:c.820C=	NP_001458.1:p.Leu274=
NM_001164278.2:c.820C=	NP_001157750.1:p.Leu274=
NM_001164279.2:c.601C=	NP_001157751.1:p.Leu201=
NM_001164280.2:c.820C=	NP_001157752.1:p.Leu274=
NM_001467.6:c.820C=	NP_001458.1:p.Leu274=
NM_001164277.2:c.820C= MANE Select	NP_001157749.1:p.Leu274=