Canonical Allele Identifier: CA6382677

Gene: WNK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.881746A>C , CM000674.2:g.881746A>C	GRCh38
NC_000012.11:g.990912A>C , CM000674.1:g.990912A>C	GRCh37
NC_000012.10:g.861173A>C	NCBI36
NG_007984.2:g.133688A>C
NG_007984.3:g.133688A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_018979.4:c.3166A>C MANE Select	NP_061852.3:p.Thr1056Pro
ENST00000315939.11:c.3166A>C MANE Select	ENSP00000313059.6:p.Thr1056Pro
NM_213655.5:c.3922A>C MANE Plus Clinical	NP_998820.3:p.Thr1308Pro
ENST00000340908.9:c.3922A>C MANE Plus Clinical	ENSP00000341292.5:p.Thr1308Pro
NM_001184985.1:c.3946A>C	NP_001171914.1:p.Thr1316Pro
NM_001184985.2:c.3946A>C	NP_001171914.1:p.Thr1316Pro
NM_014823.2:c.2425A>C	NP_055638.2:p.Thr809Pro
NM_014823.3:c.2425A>C	NP_055638.2:p.Thr809Pro
NM_018979.3:c.3166A>C	NP_061852.3:p.Thr1056Pro
NM_213655.4:c.3922A>C	NP_998820.3:p.Thr1308Pro
ENST00000315939.10:c.3166A>C	ENSP00000313059.6:p.Thr1056Pro
ENST00000340908.8:c.3922A>C	ENSP00000341292.5:p.Thr1308Pro
ENST00000530271.6:c.4405A>C	ENSP00000433548.3:p.Thr1469Pro
ENST00000535572.5:c.2425A>C	ENSP00000441972.1:p.Thr809Pro
ENST00000537687.5:c.3946A>C	ENSP00000444465.1:p.Thr1316Pro
ENST00000542543.1:n.402A>C
ENST00000544965.5:c.395A>C
ENST00000545055.1:n.276A>C
ENST00000674810.1:n.3763A>C
ENST00000675236.1:n.2061A>C
ENST00000675631.1:c.1945A>C	ENSP00000502415.1:p.Thr649Pro
ENST00000676347.1:c.613A>C	ENSP00000501875.1:p.Thr205Pro
XM_006719003.1:c.3163A>C	XP_006719066.1:p.Thr1055Pro
XM_006719003.2:c.3163A>C	XP_006719066.1:p.Thr1055Pro
XM_011520997.1:c.4405A>C	XP_011519299.1:p.Thr1469Pro
XM_011520997.3:c.4405A>C	XP_011519299.1:p.Thr1469Pro
XM_011520998.1:c.4402A>C	XP_011519300.1:p.Thr1468Pro
XM_011520998.2:c.4402A>C	XP_011519300.1:p.Thr1468Pro
XM_011520999.1:c.4405A>C	XP_011519301.1:p.Thr1469Pro
XM_011520999.2:c.4405A>C	XP_011519301.1:p.Thr1469Pro
XM_011521000.1:c.4405A>C	XP_011519302.1:p.Thr1469Pro
XM_011521000.2:c.4405A>C	XP_011519302.1:p.Thr1469Pro
XM_011521001.1:c.4126A>C	XP_011519303.1:p.Thr1376Pro
XM_011521001.2:c.4126A>C	XP_011519303.1:p.Thr1376Pro
XM_011521002.1:c.3943A>C	XP_011519304.1:p.Thr1315Pro
XM_011521002.2:c.3943A>C	XP_011519304.1:p.Thr1315Pro
XM_011521003.1:c.3667A>C	XP_011519305.1:p.Thr1223Pro
XM_011521003.2:c.3667A>C	XP_011519305.1:p.Thr1223Pro
XM_011521004.1:c.3664A>C	XP_011519306.1:p.Thr1222Pro
XM_011521004.2:c.3664A>C	XP_011519306.1:p.Thr1222Pro
XM_011521005.1:c.3184A>C	XP_011519307.1:p.Thr1062Pro
XM_011521005.2:c.3184A>C	XP_011519307.1:p.Thr1062Pro
XM_011521006.1:c.3082A>C	XP_011519308.1:p.Thr1028Pro
XM_011521006.2:c.3082A>C	XP_011519308.1:p.Thr1028Pro
XM_011521007.1:c.3079A>C	XP_011519309.1:p.Thr1027Pro
XM_011521007.2:c.3079A>C	XP_011519309.1:p.Thr1027Pro
XM_011521008.1:c.2344A>C	XP_011519310.1:p.Thr782Pro
XM_011521008.2:c.2344A>C	XP_011519310.1:p.Thr782Pro
XM_011521009.1:c.2341A>C	XP_011519311.1:p.Thr781Pro
XM_011521009.2:c.2341A>C	XP_011519311.1:p.Thr781Pro
XM_017019834.1:c.2704A>C	XP_016875323.1:p.Thr902Pro
XM_017019835.1:c.2623A>C	XP_016875324.1:p.Thr875Pro
XM_017019836.1:c.2620A>C	XP_016875325.1:p.Thr874Pro
XM_017019837.1:c.2428A>C	XP_016875326.1:p.Thr810Pro
XM_017019838.1:c.2425A>C	XP_016875327.1:p.Thr809Pro
XM_017019839.1:c.2344A>C	XP_016875328.1:p.Thr782Pro