Canonical Allele Identifier: CA2003748849

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026038G= , CM000673.2:g.119026038G=	GRCh38
NC_000011.9:g.118896748G= , CM000673.1:g.118896748G=	GRCh37
NC_000011.8:g.118401958G=	NCBI36
NG_013331.1:g.9868C= , LRG_187:g.9868C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1057C=
ENST00000697845.1:n.1837C=
ENST00000697846.1:n.1057C=
ENST00000697847.1:n.1202-281C=
ENST00000697848.1:n.1143C=
ENST00000697849.1:n.2952C=
ENST00000697850.1:n.1143C=
ENST00000697851.1:n.2751C=
ENST00000638186.1:n.1217C=
ENST00000638360.1:n.1049C=
ENST00000638925.1:n.1182C=
ENST00000650539.1:n.1319C=
ENST00000330775.9:c.913C=	ENSP00000476242.2:p.Leu305=
ENST00000357590.9:c.913C=	ENSP00000476176.2:p.Leu305=
ENST00000524428.5:n.1149C=
ENST00000525039.5:n.1337C=
ENST00000525102.5:n.1671C=
ENST00000525372.5:n.1011C=
ENST00000526275.5:n.1695C=
ENST00000527992.5:n.1141C=
ENST00000529510.5:n.601C=
ENST00000530407.5:n.1063C=
ENST00000532085.1:n.4294C=
ENST00000538950.5:c.694C=	ENSP00000475991.2:p.Leu232=
ENST00000545985.5:c.913C=	ENSP00000475241.2:p.Leu305=
NM_001164277.1:c.913C= , LRG_187t1:c.913C=	NP_001157749.1:p.Leu305=
NM_001164278.1:c.913C=	NP_001157750.1:p.Leu305=
NM_001164279.1:c.694C=	NP_001157751.1:p.Leu232=
NM_001164280.1:c.913C=	NP_001157752.1:p.Leu305=
NM_001467.5:c.913C=	NP_001458.1:p.Leu305=
NM_001164278.2:c.913C=	NP_001157750.1:p.Leu305=
NM_001164279.2:c.694C=	NP_001157751.1:p.Leu232=
NM_001164280.2:c.913C=	NP_001157752.1:p.Leu305=
NM_001467.6:c.913C=	NP_001458.1:p.Leu305=
NM_001164277.2:c.913C= MANE Select	NP_001157749.1:p.Leu305=