Canonical Allele Identifier: CA2003749351

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027042A= , CM000673.2:g.119027042A=	GRCh38
NC_000011.9:g.118897752A= , CM000673.1:g.118897752A=	GRCh37
NC_000011.8:g.118402962A=	NCBI36
NG_013331.1:g.8864T= , LRG_187:g.8864T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.909T=
ENST00000697845.1:n.833T=
ENST00000697846.1:n.909T=
ENST00000697847.1:n.909T=
ENST00000697848.1:n.909T=
ENST00000697849.1:n.1948T=
ENST00000697850.1:n.909T=
ENST00000697851.1:n.2269T=
ENST00000638186.1:n.983T=
ENST00000638360.1:n.815T=
ENST00000638925.1:n.916T=
ENST00000650539.1:n.1085T=
ENST00000330775.9:c.679T=	ENSP00000476242.2:p.Trp227=
ENST00000357590.9:c.679T=	ENSP00000476176.2:p.Trp227=
ENST00000524428.5:n.1001T=
ENST00000525039.5:n.1103T=
ENST00000525102.5:n.1437T=
ENST00000525372.5:n.680T=
ENST00000526275.5:n.1461T=
ENST00000526626.6:n.642T=
ENST00000527992.5:n.907T=
ENST00000529510.5:n.453T=
ENST00000530407.5:n.829T=
ENST00000532085.1:n.3290T=
ENST00000532888.6:n.975T=
ENST00000538950.5:c.460T=	ENSP00000475991.2:p.Trp154=
ENST00000545985.5:c.679T=	ENSP00000475241.2:p.Trp227=
NM_001164277.1:c.679T= , LRG_187t1:c.679T=	NP_001157749.1:p.Trp227=
NM_001164278.1:c.679T=	NP_001157750.1:p.Trp227=
NM_001164279.1:c.460T=	NP_001157751.1:p.Trp154=
NM_001164280.1:c.679T=	NP_001157752.1:p.Trp227=
NM_001467.5:c.679T=	NP_001458.1:p.Trp227=
NM_001164278.2:c.679T=	NP_001157750.1:p.Trp227=
NM_001164279.2:c.460T=	NP_001157751.1:p.Trp154=
NM_001164280.2:c.679T=	NP_001157752.1:p.Trp227=
NM_001467.6:c.679T=	NP_001458.1:p.Trp227=
NM_001164277.2:c.679T= MANE Select	NP_001157749.1:p.Trp227=