Canonical Allele Identifier: CA2003749661

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027665G= , CM000673.2:g.119027665G=	GRCh38
NC_000011.9:g.118898375G= , CM000673.1:g.118898375G=	GRCh37
NC_000011.8:g.118403585G=	NCBI36
NG_013331.1:g.8241C= , LRG_187:g.8241C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.818C=
ENST00000697845.1:n.742C=
ENST00000697846.1:n.818C=
ENST00000697847.1:n.818C=
ENST00000697848.1:n.818C=
ENST00000697849.1:n.1857C=
ENST00000697850.1:n.818C=
ENST00000697851.1:n.2178C=
ENST00000638186.1:n.892C=
ENST00000638360.1:n.724C=
ENST00000638925.1:n.825C=
ENST00000650539.1:n.994C=
ENST00000330775.9:c.588C=	ENSP00000476242.2:p.Leu196=
ENST00000357590.9:c.588C=	ENSP00000476176.2:p.Leu196=
ENST00000524428.5:n.910C=
ENST00000525039.5:n.1012C=
ENST00000525102.5:n.1346C=
ENST00000525372.5:n.589C=
ENST00000526275.5:n.1370C=
ENST00000526626.6:n.551C=
ENST00000527992.5:n.816C=
ENST00000529510.5:n.399+529C=
ENST00000530407.5:n.738C=
ENST00000532085.1:n.3199C=
ENST00000532888.6:n.884C=
ENST00000538950.5:c.369C=	ENSP00000475991.2:p.Leu123=
ENST00000545985.5:c.588C=	ENSP00000475241.2:p.Leu196=
NM_001164277.1:c.588C= , LRG_187t1:c.588C=	NP_001157749.1:p.Leu196=
NM_001164278.1:c.588C=	NP_001157750.1:p.Leu196=
NM_001164279.1:c.369C=	NP_001157751.1:p.Leu123=
NM_001164280.1:c.588C=	NP_001157752.1:p.Leu196=
NM_001467.5:c.588C=	NP_001458.1:p.Leu196=
NM_001164278.2:c.588C=	NP_001157750.1:p.Leu196=
NM_001164279.2:c.369C=	NP_001157751.1:p.Leu123=
NM_001164280.2:c.588C=	NP_001157752.1:p.Leu196=
NM_001467.6:c.588C=	NP_001458.1:p.Leu196=
NM_001164277.2:c.588C= MANE Select	NP_001157749.1:p.Leu196=