Canonical Allele Identifier: CA6382732

Gene: WNK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.881993A>G , CM000674.2:g.881993A>G	GRCh38
NC_000012.11:g.991159A>G , CM000674.1:g.991159A>G	GRCh37
NC_000012.10:g.861420A>G	NCBI36
NG_007984.2:g.133935A>G
NG_007984.3:g.133935A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018979.4:c.3292A>G MANE Select	NP_061852.3:p.Thr1098Ala
ENST00000315939.11:c.3292A>G MANE Select	ENSP00000313059.6:p.Thr1098Ala
NM_213655.5:c.4048A>G MANE Plus Clinical	NP_998820.3:p.Thr1350Ala
ENST00000340908.9:c.4048A>G MANE Plus Clinical	ENSP00000341292.5:p.Thr1350Ala
NM_001184985.1:c.4072A>G	NP_001171914.1:p.Thr1358Ala
NM_001184985.2:c.4072A>G	NP_001171914.1:p.Thr1358Ala
NM_014823.2:c.2551A>G	NP_055638.2:p.Thr851Ala
NM_014823.3:c.2551A>G	NP_055638.2:p.Thr851Ala
NM_018979.3:c.3292A>G	NP_061852.3:p.Thr1098Ala
NM_213655.4:c.4048A>G	NP_998820.3:p.Thr1350Ala
ENST00000315939.10:c.3292A>G	ENSP00000313059.6:p.Thr1098Ala
ENST00000340908.8:c.4048A>G	ENSP00000341292.5:p.Thr1350Ala
ENST00000530271.6:c.4531A>G	ENSP00000433548.3:p.Thr1511Ala
ENST00000534872.1:c.109A>G	ENSP00000446253.1:p.Thr37Ala
ENST00000535572.5:c.2551A>G	ENSP00000441972.1:p.Thr851Ala
ENST00000537687.5:c.4072A>G	ENSP00000444465.1:p.Thr1358Ala
ENST00000544965.5:c.521A>G
ENST00000545055.1:n.402A>G
ENST00000674810.1:n.3889A>G
ENST00000675236.1:n.2187A>G
ENST00000675631.1:c.2071A>G	ENSP00000502415.1:p.Thr691Ala
ENST00000676347.1:c.739A>G	ENSP00000501875.1:p.Thr247Ala
XM_006719003.1:c.3289A>G	XP_006719066.1:p.Thr1097Ala
XM_006719003.2:c.3289A>G	XP_006719066.1:p.Thr1097Ala
XM_011520997.1:c.4531A>G	XP_011519299.1:p.Thr1511Ala
XM_011520997.3:c.4531A>G	XP_011519299.1:p.Thr1511Ala
XM_011520998.1:c.4528A>G	XP_011519300.1:p.Thr1510Ala
XM_011520998.2:c.4528A>G	XP_011519300.1:p.Thr1510Ala
XM_011520999.1:c.4531A>G	XP_011519301.1:p.Thr1511Ala
XM_011520999.2:c.4531A>G	XP_011519301.1:p.Thr1511Ala
XM_011521000.1:c.4531A>G	XP_011519302.1:p.Thr1511Ala
XM_011521000.2:c.4531A>G	XP_011519302.1:p.Thr1511Ala
XM_011521001.1:c.4252A>G	XP_011519303.1:p.Thr1418Ala
XM_011521001.2:c.4252A>G	XP_011519303.1:p.Thr1418Ala
XM_011521002.1:c.4069A>G	XP_011519304.1:p.Thr1357Ala
XM_011521002.2:c.4069A>G	XP_011519304.1:p.Thr1357Ala
XM_011521003.1:c.3793A>G	XP_011519305.1:p.Thr1265Ala
XM_011521003.2:c.3793A>G	XP_011519305.1:p.Thr1265Ala
XM_011521004.1:c.3790A>G	XP_011519306.1:p.Thr1264Ala
XM_011521004.2:c.3790A>G	XP_011519306.1:p.Thr1264Ala
XM_011521005.1:c.3310A>G	XP_011519307.1:p.Thr1104Ala
XM_011521005.2:c.3310A>G	XP_011519307.1:p.Thr1104Ala
XM_011521006.1:c.3208A>G	XP_011519308.1:p.Thr1070Ala
XM_011521006.2:c.3208A>G	XP_011519308.1:p.Thr1070Ala
XM_011521007.1:c.3205A>G	XP_011519309.1:p.Thr1069Ala
XM_011521007.2:c.3205A>G	XP_011519309.1:p.Thr1069Ala
XM_011521008.1:c.2470A>G	XP_011519310.1:p.Thr824Ala
XM_011521008.2:c.2470A>G	XP_011519310.1:p.Thr824Ala
XM_011521009.1:c.2467A>G	XP_011519311.1:p.Thr823Ala
XM_011521009.2:c.2467A>G	XP_011519311.1:p.Thr823Ala
XM_017019834.1:c.2830A>G	XP_016875323.1:p.Thr944Ala
XM_017019835.1:c.2749A>G	XP_016875324.1:p.Thr917Ala
XM_017019836.1:c.2746A>G	XP_016875325.1:p.Thr916Ala
XM_017019837.1:c.2554A>G	XP_016875326.1:p.Thr852Ala
XM_017019838.1:c.2551A>G	XP_016875327.1:p.Thr851Ala
XM_017019839.1:c.2470A>G	XP_016875328.1:p.Thr824Ala