Canonical Allele Identifier: CA2003749330

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026997A= , CM000673.2:g.119026997A=	GRCh38
NC_000011.9:g.118897707A= , CM000673.1:g.118897707A=	GRCh37
NC_000011.8:g.118402917A=	NCBI36
NG_013331.1:g.8909T= , LRG_187:g.8909T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.954T=
ENST00000697845.1:n.878T=
ENST00000697846.1:n.954T=
ENST00000697847.1:n.954T=
ENST00000697848.1:n.954T=
ENST00000697849.1:n.1993T=
ENST00000697850.1:n.954T=
ENST00000697851.1:n.2314T=
ENST00000638186.1:n.1028T=
ENST00000638360.1:n.860T=
ENST00000638925.1:n.961T=
ENST00000650539.1:n.1130T=
ENST00000330775.9:c.724T=	ENSP00000476242.2:p.Cys242=
ENST00000357590.9:c.724T=	ENSP00000476176.2:p.Cys242=
ENST00000524428.5:n.1046T=
ENST00000525039.5:n.1148T=
ENST00000525102.5:n.1482T=
ENST00000525372.5:n.725T=
ENST00000526275.5:n.1506T=
ENST00000526626.6:n.687T=
ENST00000527992.5:n.952T=
ENST00000529510.5:n.498T=
ENST00000530407.5:n.874T=
ENST00000532085.1:n.3335T=
ENST00000532888.6:n.1020T=
ENST00000538950.5:c.505T=	ENSP00000475991.2:p.Cys169=
ENST00000545985.5:c.724T=	ENSP00000475241.2:p.Cys242=
NM_001164277.1:c.724T= , LRG_187t1:c.724T=	NP_001157749.1:p.Cys242=
NM_001164278.1:c.724T=	NP_001157750.1:p.Cys242=
NM_001164279.1:c.505T=	NP_001157751.1:p.Cys169=
NM_001164280.1:c.724T=	NP_001157752.1:p.Cys242=
NM_001467.5:c.724T=	NP_001458.1:p.Cys242=
NM_001164278.2:c.724T=	NP_001157750.1:p.Cys242=
NM_001164279.2:c.505T=	NP_001157751.1:p.Cys169=
NM_001164280.2:c.724T=	NP_001157752.1:p.Cys242=
NM_001467.6:c.724T=	NP_001458.1:p.Cys242=
NM_001164277.2:c.724T= MANE Select	NP_001157749.1:p.Cys242=