Canonical Allele Identifier: CA1978109595

Gene: SLC22A24

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.63137510A= , CM000673.2:g.63137510A=	GRCh38
NC_000011.9:g.62904982A= , CM000673.1:g.62904982A=	GRCh37
NC_000011.8:g.62661558A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000326192.5:c.403-2742T=	ENSP00000321549.5:n.403-2742T=
ENST00000417740.5:c.403-2742T=	ENSP00000396586.1:n.403-2742T=
ENST00000612278.4:c.403-2742T= MANE Select	ENSP00000480336.1:n.403-2742T=
NM_001136506.2:c.403-2742T= MANE Select	NP_001129978.2:n.403-2742T=
NM_173586.2:c.403-2742T=	NP_775857.2:n.403-2742T=
XM_011544964.1:c.403-2742T=	XP_011543266.1:n.403-2742T=
XM_011544965.1:c.403-2742T=	XP_011543267.1:n.403-2742T=
XM_011544966.1:c.403-2742T=	XP_011543268.1:n.403-2742T=
XM_011544967.1:c.403-2742T=	XP_011543269.1:n.403-2742T=
NM_173586.3:c.403-2742T=	NP_775857.2:n.403-2742T=