Canonical Allele Identifier: CA37770107

Gene: KCNK2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215216266T>C , CM000663.2:g.215216266T>C	GRCh38
NC_000001.10:g.215389609T>C , CM000663.1:g.215389609T>C	GRCh37
NC_000001.9:g.213456232T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000444842.7:c.964-18562T>C MANE Select	ENSP00000394033.2:n.964-18562T>C
ENST00000391894.6:c.919-18562T>C	ENSP00000375764.2:n.919-18562T>C
ENST00000391895.6:c.952-18562T>C	ENSP00000375765.2:n.952-18562T>C
ENST00000444842.6:c.964-18562T>C	ENSP00000394033.2:n.964-18562T>C
ENST00000467031.5:c.*78-18562T>C	ENSP00000420203.1:n.*78-18562T>C
ENST00000474771.5:c.*78-18562T>C	ENSP00000420499.1:n.*78-18562T>C
ENST00000486921.5:c.*375-18562T>C	ENSP00000418706.1:n.*375-18562T>C
NM_001017424.2:c.952-18562T>C	NP_001017424.1:n.952-18562T>C
NM_001017425.2:c.964-18562T>C	NP_001017425.2:n.964-18562T>C
NM_014217.3:c.919-18562T>C	NP_055032.1:n.919-18562T>C
XM_011509521.1:c.922-18562T>C	XP_011507823.1:n.922-18562T>C
XM_011509522.1:c.796-18562T>C	XP_011507824.1:n.796-18562T>C
XM_011509523.1:c.796-18562T>C	XP_011507825.1:n.796-18562T>C
XM_011509524.1:c.796-18562T>C	XP_011507826.1:n.796-18562T>C
XM_011509522.2:c.796-18562T>C	XP_011507824.1:n.796-18562T>C
XM_011509524.2:c.796-18562T>C	XP_011507826.1:n.796-18562T>C
XM_017001248.1:c.952-18562T>C	XP_016856737.1:n.952-18562T>C
XM_017001249.1:c.922-18562T>C	XP_016856738.1:n.922-18562T>C
NM_001017424.3:c.952-18562T>C	NP_001017424.1:n.952-18562T>C
NM_001017425.3:c.964-18562T>C MANE Select	NP_001017425.2:n.964-18562T>C
NM_014217.4:c.919-18562T>C	NP_055032.1:n.919-18562T>C