Canonical Allele Identifier: CA731313876

Gene: KCNK2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215236763G>T , CM000663.2:g.215236763G>T	GRCh38
NC_000001.10:g.215410106G>T , CM000663.1:g.215410106G>T	GRCh37
NC_000001.9:g.213476729G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000444842.7:c.*1618G>T MANE Select	ENSP00000394033.2:n.*1618G>T
ENST00000444842.6:c.*1618G>T	ENSP00000394033.2:n.*1618G>T
NM_001017424.2:c.*1618G>T	NP_001017424.1:n.*1618G>T
NM_001017425.2:c.*1618G>T	NP_001017425.2:n.*1618G>T
NM_014217.3:c.*1618G>T	NP_055032.1:n.*1618G>T
XM_011509521.1:c.*1618G>T	XP_011507823.1:n.*1618G>T
XM_011509522.1:c.*1618G>T	XP_011507824.1:n.*1618G>T
XM_011509523.1:c.*1618G>T	XP_011507825.1:n.*1618G>T
XM_011509524.1:c.*1618G>T	XP_011507826.1:n.*1618G>T
XM_011509522.2:c.*1618G>T	XP_011507824.1:n.*1618G>T
XM_011509524.2:c.*1618G>T	XP_011507826.1:n.*1618G>T
XM_017001248.1:c.*1618G>T	XP_016856737.1:n.*1618G>T
XM_017001249.1:c.*1618G>T	XP_016856738.1:n.*1618G>T
NM_001017424.3:c.*1618G>T	NP_001017424.1:n.*1618G>T
NM_001017425.3:c.*1618G>T MANE Select	NP_001017425.2:n.*1618G>T
NM_014217.4:c.*1618G>T	NP_055032.1:n.*1618G>T