Canonical Allele Identifier: CA679253945

Gene: SLC22A11

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64563990A>T , CM000673.2:g.64563990A>T	GRCh38
NC_000011.9:g.64331462A>T , CM000673.1:g.64331462A>T	GRCh37
NC_000011.8:g.64088038A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301891.9:c.822-318A>T MANE Select	ENSP00000301891.4:n.822-318A>T
ENST00000301891.8:c.822-318A>T	ENSP00000301891.4:n.822-318A>T
ENST00000377581.7:c.822-318A>T	ENSP00000366804.3:n.822-318A>T
ENST00000377585.7:c.822-318A>T	ENSP00000366809.3:n.822-318A>T
ENST00000460745.1:n.247-318A>T
ENST00000478051.5:n.855-1232A>T
ENST00000490834.5:n.751-1232A>T
NM_001307985.1:c.822-318A>T	NP_001294914.1:n.822-318A>T
NM_018484.2:c.822-318A>T	NP_060954.1:n.822-318A>T
NM_018484.3:c.822-318A>T	NP_060954.1:n.822-318A>T
XM_011545167.1:c.423-318A>T	XP_011543469.1:n.423-318A>T
NM_001307985.2:c.822-318A>T	NP_001294914.1:n.822-318A>T
NM_018484.4:c.822-318A>T MANE Select	NP_060954.1:n.822-318A>T