Canonical Allele Identifier: CA338641280

Gene: CLCNKB

Linked Data

• gnomAD v4: 1-16051712-G-C
• MyVariant Identifiers: chr1:g.16378207G>C (hg19) ; chr1:g.16051712G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051712G>C , CM000663.2:g.16051712G>C	GRCh38
NC_000001.10:g.16378207G>C , CM000663.1:g.16378207G>C	GRCh37
NC_000001.9:g.16250794G>C	NCBI36
NG_013079.1:g.12961G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682338.1:c.1300G>C	ENSP00000507062.1:p.Ala434Pro
ENST00000682793.1:c.1300G>C	ENSP00000506910.1:p.Ala434Pro
ENST00000682838.1:c.*1042G>C	ENSP00000507652.1:n.*1042G>C
ENST00000683578.1:c.1300G>C	ENSP00000507430.1:p.Ala434Pro
ENST00000683606.1:n.915G>C
ENST00000683661.1:n.2835G>C
ENST00000684324.1:c.1300G>C	ENSP00000507937.1:p.Ala434Pro
ENST00000684545.1:c.1300G>C	ENSP00000506733.1:p.Ala434Pro
ENST00000684624.1:n.677G>C
ENST00000684714.1:c.1300G>C	ENSP00000506861.1:p.Ala434Pro
ENST00000684731.1:n.761G>C
ENST00000375679.9:c.1300G>C MANE Select	ENSP00000364831.5:p.Ala434Pro
ENST00000375667.7:c.793G>C	ENSP00000364819.3:p.Ala265Pro
ENST00000375679.8:c.1300G>C	ENSP00000364831.4:p.Ala434Pro
ENST00000619181.4:c.919G>C	ENSP00000483866.1:p.Ala307Pro
NM_000085.4:c.1300G>C	NP_000076.2:p.Ala434Pro
NM_001165945.2:c.793G>C	NP_001159417.2:p.Ala265Pro
XM_011540619.1:c.1141G>C	XP_011538921.1:p.Ala381Pro
XM_011540620.1:c.1300G>C	XP_011538922.1:p.Ala434Pro
XM_011540621.1:c.649G>C	XP_011538923.1:p.Ala217Pro
NM_000085.5:c.1300G>C MANE Select	NP_000076.2:p.Ala434Pro