Canonical Allele Identifier: CA2003749706

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027732T= , CM000673.2:g.119027732T=	GRCh38
NC_000011.9:g.118898442T= , CM000673.1:g.118898442T=	GRCh37
NC_000011.8:g.118403652T=	NCBI36
NG_013331.1:g.8175A= , LRG_187:g.8175A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.751A=
ENST00000697845.1:n.675A=
ENST00000697846.1:n.751A=
ENST00000697847.1:n.751A=
ENST00000697848.1:n.751A=
ENST00000697849.1:n.1790A=
ENST00000697850.1:n.751A=
ENST00000697851.1:n.2111A=
ENST00000638186.1:n.825A=
ENST00000638360.1:n.657A=
ENST00000638925.1:n.758A=
ENST00000650539.1:n.927A=
ENST00000330775.9:c.522A=	ENSP00000476242.2:p.Ala174=
ENST00000357590.9:c.522A=	ENSP00000476176.2:p.Ala174=
ENST00000524428.5:n.843A=
ENST00000525039.5:n.945A=
ENST00000525102.5:n.1279A=
ENST00000525372.5:n.522A=
ENST00000526275.5:n.1303A=
ENST00000526626.6:n.484A=
ENST00000527992.5:n.749A=
ENST00000529510.5:n.399+462A=
ENST00000530407.5:n.671A=
ENST00000532085.1:n.3132A=
ENST00000532888.6:n.817A=
ENST00000538950.5:c.303A=	ENSP00000475991.2:p.Ala101=
ENST00000545985.5:c.522A=	ENSP00000475241.2:p.Ala174=
NM_001164277.1:c.522A= , LRG_187t1:c.522A=	NP_001157749.1:p.Ala174=
NM_001164278.1:c.522A=	NP_001157750.1:p.Ala174=
NM_001164279.1:c.303A=	NP_001157751.1:p.Ala101=
NM_001164280.1:c.522A=	NP_001157752.1:p.Ala174=
NM_001467.5:c.522A=	NP_001458.1:p.Ala174=
NM_001164278.2:c.522A=	NP_001157750.1:p.Ala174=
NM_001164279.2:c.303A=	NP_001157751.1:p.Ala101=
NM_001164280.2:c.522A=	NP_001157752.1:p.Ala174=
NM_001467.6:c.522A=	NP_001458.1:p.Ala174=
NM_001164277.2:c.522A= MANE Select	NP_001157749.1:p.Ala174=