Canonical Allele Identifier: CA2003750025

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028348G= , CM000673.2:g.119028348G=	GRCh38
NC_000011.9:g.118899058G= , CM000673.1:g.118899058G=	GRCh37
NC_000011.8:g.118404268G=	NCBI36
NG_013331.1:g.7559C= , LRG_187:g.7559C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.456C=
ENST00000697845.1:n.380C=
ENST00000697846.1:n.456C=
ENST00000697847.1:n.456C=
ENST00000697848.1:n.456C=
ENST00000697849.1:n.1495C=
ENST00000697850.1:n.456C=
ENST00000697851.1:n.1495C=
ENST00000638186.1:n.530C=
ENST00000638360.1:n.464C=
ENST00000638925.1:n.463C=
ENST00000650539.1:n.632C=
ENST00000330775.9:c.227C=	ENSP00000476242.2:p.Ala76=
ENST00000357590.9:c.227C=	ENSP00000476176.2:p.Ala76=
ENST00000524428.5:n.227C=
ENST00000525039.5:n.650C=
ENST00000525102.5:n.984C=
ENST00000525372.5:n.227C=
ENST00000525787.1:n.522C=
ENST00000526275.5:n.687C=
ENST00000526626.6:n.344-476C=
ENST00000527992.5:n.454C=
ENST00000529510.5:n.245C=
ENST00000530407.5:n.376C=
ENST00000532085.1:n.2516C=
ENST00000532888.6:n.522C=
ENST00000534384.1:n.447C=
ENST00000538950.5:c.8C=	ENSP00000475991.2:p.Ala3=
ENST00000545985.5:c.227C=	ENSP00000475241.2:p.Ala76=
NM_001164277.1:c.227C= , LRG_187t1:c.227C=	NP_001157749.1:p.Ala76=
NM_001164278.1:c.227C=	NP_001157750.1:p.Ala76=
NM_001164279.1:c.8C=	NP_001157751.1:p.Ala3=
NM_001164280.1:c.227C=	NP_001157752.1:p.Ala76=
NM_001467.5:c.227C=	NP_001458.1:p.Ala76=
NM_001164278.2:c.227C=	NP_001157750.1:p.Ala76=
NM_001164279.2:c.8C=	NP_001157751.1:p.Ala3=
NM_001164280.2:c.227C=	NP_001157752.1:p.Ala76=
NM_001467.6:c.227C=	NP_001458.1:p.Ala76=
NM_001164277.2:c.227C= MANE Select	NP_001157749.1:p.Ala76=