Canonical Allele Identifier: CA2003748868

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026066G= , CM000673.2:g.119026066G=	GRCh38
NC_000011.9:g.118896776G= , CM000673.1:g.118896776G=	GRCh37
NC_000011.8:g.118401986G=	NCBI36
NG_013331.1:g.9840C= , LRG_187:g.9840C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1029C=
ENST00000697845.1:n.1809C=
ENST00000697846.1:n.1029C=
ENST00000697847.1:n.1202-309C=
ENST00000697848.1:n.1115C=
ENST00000697849.1:n.2924C=
ENST00000697850.1:n.1115C=
ENST00000697851.1:n.2723C=
ENST00000638186.1:n.1189C=
ENST00000638360.1:n.1021C=
ENST00000638925.1:n.1154C=
ENST00000650539.1:n.1291C=
ENST00000330775.9:c.885C=	ENSP00000476242.2:p.Asn295=
ENST00000357590.9:c.885C=	ENSP00000476176.2:p.Asn295=
ENST00000524428.5:n.1121C=
ENST00000525039.5:n.1309C=
ENST00000525102.5:n.1643C=
ENST00000525372.5:n.983C=
ENST00000526275.5:n.1667C=
ENST00000527992.5:n.1113C=
ENST00000529510.5:n.573C=
ENST00000530407.5:n.1035C=
ENST00000532085.1:n.4266C=
ENST00000538950.5:c.666C=	ENSP00000475991.2:p.Asn222=
ENST00000545985.5:c.885C=	ENSP00000475241.2:p.Asn295=
NM_001164277.1:c.885C= , LRG_187t1:c.885C=	NP_001157749.1:p.Asn295=
NM_001164278.1:c.885C=	NP_001157750.1:p.Asn295=
NM_001164279.1:c.666C=	NP_001157751.1:p.Asn222=
NM_001164280.1:c.885C=	NP_001157752.1:p.Asn295=
NM_001467.5:c.885C=	NP_001458.1:p.Asn295=
NM_001164278.2:c.885C=	NP_001157750.1:p.Asn295=
NM_001164279.2:c.666C=	NP_001157751.1:p.Asn222=
NM_001164280.2:c.885C=	NP_001157752.1:p.Asn295=
NM_001467.6:c.885C=	NP_001458.1:p.Asn295=
NM_001164277.2:c.885C= MANE Select	NP_001157749.1:p.Asn295=