Canonical Allele Identifier: CA2003749756

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027826G= , CM000673.2:g.119027826G=	GRCh38
NC_000011.9:g.118898536G= , CM000673.1:g.118898536G=	GRCh37
NC_000011.8:g.118403746G=	NCBI36
NG_013331.1:g.8081C= , LRG_187:g.8081C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.657C=
ENST00000697845.1:n.581C=
ENST00000697846.1:n.657C=
ENST00000697847.1:n.657C=
ENST00000697848.1:n.657C=
ENST00000697849.1:n.1696C=
ENST00000697850.1:n.657C=
ENST00000697851.1:n.2017C=
ENST00000638186.1:n.731C=
ENST00000638360.1:n.619-56C=
ENST00000638925.1:n.664C=
ENST00000650539.1:n.833C=
ENST00000330775.9:c.428C=	ENSP00000476242.2:p.Thr143=
ENST00000357590.9:c.428C=	ENSP00000476176.2:p.Thr143=
ENST00000524428.5:n.749C=
ENST00000525039.5:n.851C=
ENST00000525102.5:n.1185C=
ENST00000525372.5:n.428C=
ENST00000525787.1:n.1044C=
ENST00000526275.5:n.1209C=
ENST00000526626.6:n.390C=
ENST00000527992.5:n.655C=
ENST00000529510.5:n.399+368C=
ENST00000530407.5:n.577C=
ENST00000532085.1:n.3038C=
ENST00000532888.6:n.723C=
ENST00000538950.5:c.209C=	ENSP00000475991.2:p.Thr70=
ENST00000545985.5:c.428C=	ENSP00000475241.2:p.Thr143=
NM_001164277.1:c.428C= , LRG_187t1:c.428C=	NP_001157749.1:p.Thr143=
NM_001164278.1:c.428C=	NP_001157750.1:p.Thr143=
NM_001164279.1:c.209C=	NP_001157751.1:p.Thr70=
NM_001164280.1:c.428C=	NP_001157752.1:p.Thr143=
NM_001467.5:c.428C=	NP_001458.1:p.Thr143=
NM_001164278.2:c.428C=	NP_001157750.1:p.Thr143=
NM_001164279.2:c.209C=	NP_001157751.1:p.Thr70=
NM_001164280.2:c.428C=	NP_001157752.1:p.Thr143=
NM_001467.6:c.428C=	NP_001458.1:p.Thr143=
NM_001164277.2:c.428C= MANE Select	NP_001157749.1:p.Thr143=