Canonical Allele Identifier: CA1978817060

Gene: SLC22A11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64566642C= , CM000673.2:g.64566642C=	GRCh38
NC_000011.9:g.64334114C= , CM000673.1:g.64334114C=	GRCh37
NC_000011.8:g.64090690C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018484.4:c.1059-957C= MANE Select	NP_060954.1:n.1059-957C=
ENST00000301891.9:c.1059-957C= MANE Select	ENSP00000301891.4:n.1059-957C=
NM_001307985.1:c.1058+1305C=	NP_001294914.1:n.1058+1305C=
NM_001307985.2:c.1058+1305C=	NP_001294914.1:n.1058+1305C=
NM_018484.2:c.1059-957C=	NP_060954.1:n.1059-957C=
NM_018484.3:c.1059-957C=	NP_060954.1:n.1059-957C=
ENST00000301891.8:c.1059-957C=	ENSP00000301891.4:n.1059-957C=
ENST00000377581.7:c.1059-957C=	ENSP00000366804.3:n.1059-957C=
ENST00000377585.7:c.1058+1305C=	ENSP00000366809.3:n.1058+1305C=
ENST00000460745.1:n.1788C=
XM_011545167.1:c.660-957C=	XP_011543469.1:n.660-957C=