Canonical Allele Identifier: CA2003749655

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027658G= , CM000673.2:g.119027658G=	GRCh38
NC_000011.9:g.118898368G= , CM000673.1:g.118898368G=	GRCh37
NC_000011.8:g.118403578G=	NCBI36
NG_013331.1:g.8248C= , LRG_187:g.8248C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.825C=
ENST00000697845.1:n.749C=
ENST00000697846.1:n.825C=
ENST00000697847.1:n.825C=
ENST00000697848.1:n.825C=
ENST00000697849.1:n.1864C=
ENST00000697850.1:n.825C=
ENST00000697851.1:n.2185C=
ENST00000638186.1:n.899C=
ENST00000638360.1:n.731C=
ENST00000638925.1:n.832C=
ENST00000650539.1:n.1001C=
ENST00000330775.9:c.595C=	ENSP00000476242.2:p.Leu199=
ENST00000357590.9:c.595C=	ENSP00000476176.2:p.Leu199=
ENST00000524428.5:n.917C=
ENST00000525039.5:n.1019C=
ENST00000525102.5:n.1353C=
ENST00000525372.5:n.596C=
ENST00000526275.5:n.1377C=
ENST00000526626.6:n.558C=
ENST00000527992.5:n.823C=
ENST00000529510.5:n.399+536C=
ENST00000530407.5:n.745C=
ENST00000532085.1:n.3206C=
ENST00000532888.6:n.891C=
ENST00000538950.5:c.376C=	ENSP00000475991.2:p.Leu126=
ENST00000545985.5:c.595C=	ENSP00000475241.2:p.Leu199=
NM_001164277.1:c.595C= , LRG_187t1:c.595C=	NP_001157749.1:p.Leu199=
NM_001164278.1:c.595C=	NP_001157750.1:p.Leu199=
NM_001164279.1:c.376C=	NP_001157751.1:p.Leu126=
NM_001164280.1:c.595C=	NP_001157752.1:p.Leu199=
NM_001467.5:c.595C=	NP_001458.1:p.Leu199=
NM_001164278.2:c.595C=	NP_001157750.1:p.Leu199=
NM_001164279.2:c.376C=	NP_001157751.1:p.Leu126=
NM_001164280.2:c.595C=	NP_001157752.1:p.Leu199=
NM_001467.6:c.595C=	NP_001458.1:p.Leu199=
NM_001164277.2:c.595C= MANE Select	NP_001157749.1:p.Leu199=