Canonical Allele Identifier: CA2003775093

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029301C= , CM000673.2:g.119029301C=	GRCh38
NC_000011.9:g.118900011C= , CM000673.1:g.118900011C=	GRCh37
NC_000011.8:g.118405221C=	NCBI36
NG_013331.1:g.6606G= , LRG_187:g.6606G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.298G=
ENST00000697846.1:n.298G=
ENST00000697847.1:n.298G=
ENST00000697848.1:n.298G=
ENST00000697849.1:n.542G=
ENST00000697850.1:n.298G=
ENST00000697851.1:n.542G=
ENST00000638186.1:n.372G=
ENST00000638360.1:n.306G=
ENST00000638925.1:n.305G=
ENST00000650539.1:n.474G=
ENST00000330775.9:c.69G=	ENSP00000476242.2:p.Leu23=
ENST00000357590.9:c.69G=	ENSP00000476176.2:p.Leu23=
ENST00000524428.5:n.69G=
ENST00000525039.5:n.492G=
ENST00000525102.5:n.826G=
ENST00000525372.5:n.69G=
ENST00000525787.1:n.364G=
ENST00000526626.6:n.264G=
ENST00000527992.5:n.296G=
ENST00000529510.5:n.87G=
ENST00000530407.5:n.197+91G=
ENST00000532085.1:n.1563G=
ENST00000532888.6:n.264G=
ENST00000534384.1:n.289G=
ENST00000538950.5:c.-172+91G=	ENSP00000475991.2:n.-172+91G=
ENST00000545985.5:c.69G=	ENSP00000475241.2:p.Leu23=
NM_001164277.1:c.69G= , LRG_187t1:c.69G=	NP_001157749.1:p.Leu23=
NM_001164278.1:c.69G=	NP_001157750.1:p.Leu23=
NM_001164279.1:c.-172+91G=	NP_001157751.1:n.-172+91G=
NM_001164280.1:c.69G=	NP_001157752.1:p.Leu23=
NM_001467.5:c.69G=	NP_001458.1:p.Leu23=
NM_001164278.2:c.69G=	NP_001157750.1:p.Leu23=
NM_001164279.2:c.-172+91G=	NP_001157751.1:n.-172+91G=
NM_001164280.2:c.69G=	NP_001157752.1:p.Leu23=
NM_001467.6:c.69G=	NP_001458.1:p.Leu23=
NM_001164277.2:c.69G= MANE Select	NP_001157749.1:p.Leu23=