Canonical Allele Identifier: CA2003748875

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026078C= , CM000673.2:g.119026078C=	GRCh38
NC_000011.9:g.118896788C= , CM000673.1:g.118896788C=	GRCh37
NC_000011.8:g.118401998C=	NCBI36
NG_013331.1:g.9828G= , LRG_187:g.9828G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1017G=
ENST00000697845.1:n.1797G=
ENST00000697846.1:n.1017G=
ENST00000697847.1:n.1202-321G=
ENST00000697848.1:n.1103G=
ENST00000697849.1:n.2912G=
ENST00000697850.1:n.1103G=
ENST00000697851.1:n.2711G=
ENST00000638186.1:n.1177G=
ENST00000638360.1:n.1009G=
ENST00000638925.1:n.1142G=
ENST00000650539.1:n.1279G=
ENST00000330775.9:c.873G=	ENSP00000476242.2:p.Ala291=
ENST00000357590.9:c.873G=	ENSP00000476176.2:p.Ala291=
ENST00000524428.5:n.1109G=
ENST00000525039.5:n.1297G=
ENST00000525102.5:n.1631G=
ENST00000525372.5:n.971G=
ENST00000526275.5:n.1655G=
ENST00000527992.5:n.1101G=
ENST00000529510.5:n.561G=
ENST00000530407.5:n.1023G=
ENST00000532085.1:n.4254G=
ENST00000538950.5:c.654G=	ENSP00000475991.2:p.Ala218=
ENST00000545985.5:c.873G=	ENSP00000475241.2:p.Ala291=
NM_001164277.1:c.873G= , LRG_187t1:c.873G=	NP_001157749.1:p.Ala291=
NM_001164278.1:c.873G=	NP_001157750.1:p.Ala291=
NM_001164279.1:c.654G=	NP_001157751.1:p.Ala218=
NM_001164280.1:c.873G=	NP_001157752.1:p.Ala291=
NM_001467.5:c.873G=	NP_001458.1:p.Ala291=
NM_001164278.2:c.873G=	NP_001157750.1:p.Ala291=
NM_001164279.2:c.654G=	NP_001157751.1:p.Ala218=
NM_001164280.2:c.873G=	NP_001157752.1:p.Ala291=
NM_001467.6:c.873G=	NP_001458.1:p.Ala291=
NM_001164277.2:c.873G= MANE Select	NP_001157749.1:p.Ala291=