Canonical Allele Identifier: CA2003749689

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027716G= , CM000673.2:g.119027716G=	GRCh38
NC_000011.9:g.118898426G= , CM000673.1:g.118898426G=	GRCh37
NC_000011.8:g.118403636G=	NCBI36
NG_013331.1:g.8190C= , LRG_187:g.8190C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.767C=
ENST00000697845.1:n.691C=
ENST00000697846.1:n.767C=
ENST00000697847.1:n.767C=
ENST00000697848.1:n.767C=
ENST00000697849.1:n.1806C=
ENST00000697850.1:n.767C=
ENST00000697851.1:n.2127C=
ENST00000638186.1:n.841C=
ENST00000638360.1:n.673C=
ENST00000638925.1:n.774C=
ENST00000650539.1:n.943C=
ENST00000330775.9:c.537C=	ENSP00000476242.2:p.Val179=
ENST00000357590.9:c.537C=	ENSP00000476176.2:p.Val179=
ENST00000524428.5:n.859C=
ENST00000525039.5:n.961C=
ENST00000525102.5:n.1295C=
ENST00000525372.5:n.538C=
ENST00000526275.5:n.1319C=
ENST00000526626.6:n.500C=
ENST00000527992.5:n.765C=
ENST00000529510.5:n.399+478C=
ENST00000530407.5:n.687C=
ENST00000532085.1:n.3148C=
ENST00000532888.6:n.833C=
ENST00000538950.5:c.318C=	ENSP00000475991.2:p.Val106=
ENST00000545985.5:c.537C=	ENSP00000475241.2:p.Val179=
NM_001164277.1:c.537C= , LRG_187t1:c.537C=	NP_001157749.1:p.Val179=
NM_001164278.1:c.537C=	NP_001157750.1:p.Val179=
NM_001164279.1:c.318C=	NP_001157751.1:p.Val106=
NM_001164280.1:c.537C=	NP_001157752.1:p.Val179=
NM_001467.5:c.537C=	NP_001458.1:p.Val179=
NM_001164278.2:c.537C=	NP_001157750.1:p.Val179=
NM_001164279.2:c.318C=	NP_001157751.1:p.Val106=
NM_001164280.2:c.537C=	NP_001157752.1:p.Val179=
NM_001467.6:c.537C=	NP_001458.1:p.Val179=
NM_001164277.2:c.537C= MANE Select	NP_001157749.1:p.Val179=