Canonical Allele Identifier: CA2003749318

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026974G= , CM000673.2:g.119026974G=	GRCh38
NC_000011.9:g.118897684G= , CM000673.1:g.118897684G=	GRCh37
NC_000011.8:g.118402894G=	NCBI36
NG_013331.1:g.8932C= , LRG_187:g.8932C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.977C=
ENST00000697845.1:n.901C=
ENST00000697846.1:n.977C=
ENST00000697847.1:n.977C=
ENST00000697848.1:n.977C=
ENST00000697849.1:n.2016C=
ENST00000697850.1:n.977C=
ENST00000697851.1:n.2337C=
ENST00000638186.1:n.1051C=
ENST00000638360.1:n.883C=
ENST00000638925.1:n.984C=
ENST00000650539.1:n.1153C=
ENST00000330775.9:c.747C=	ENSP00000476242.2:p.Phe249=
ENST00000357590.9:c.747C=	ENSP00000476176.2:p.Phe249=
ENST00000524428.5:n.1069C=
ENST00000525039.5:n.1171C=
ENST00000525102.5:n.1505C=
ENST00000525372.5:n.748C=
ENST00000526275.5:n.1529C=
ENST00000526626.6:n.710C=
ENST00000527992.5:n.975C=
ENST00000529510.5:n.521C=
ENST00000530407.5:n.897C=
ENST00000532085.1:n.3358C=
ENST00000532888.6:n.1043C=
ENST00000538950.5:c.528C=	ENSP00000475991.2:p.Phe176=
ENST00000545985.5:c.747C=	ENSP00000475241.2:p.Phe249=
NM_001164277.1:c.747C= , LRG_187t1:c.747C=	NP_001157749.1:p.Phe249=
NM_001164278.1:c.747C=	NP_001157750.1:p.Phe249=
NM_001164279.1:c.528C=	NP_001157751.1:p.Phe176=
NM_001164280.1:c.747C=	NP_001157752.1:p.Phe249=
NM_001467.5:c.747C=	NP_001458.1:p.Phe249=
NM_001164278.2:c.747C=	NP_001157750.1:p.Phe249=
NM_001164279.2:c.528C=	NP_001157751.1:p.Phe176=
NM_001164280.2:c.747C=	NP_001157752.1:p.Phe249=
NM_001467.6:c.747C=	NP_001458.1:p.Phe249=
NM_001164277.2:c.747C= MANE Select	NP_001157749.1:p.Phe249=