Canonical Allele Identifier: CA383327635

Gene: WNK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.881747C>G , CM000674.2:g.881747C>G	GRCh38
NC_000012.11:g.990913C>G , CM000674.1:g.990913C>G	GRCh37
NC_000012.10:g.861174C>G	NCBI36
NG_007984.2:g.133689C>G
NG_007984.3:g.133689C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018979.4:c.3167C>G MANE Select	NP_061852.3:p.Thr1056Ser
ENST00000315939.11:c.3167C>G MANE Select	ENSP00000313059.6:p.Thr1056Ser
NM_213655.5:c.3923C>G MANE Plus Clinical	NP_998820.3:p.Thr1308Ser
ENST00000340908.9:c.3923C>G MANE Plus Clinical	ENSP00000341292.5:p.Thr1308Ser
NM_001184985.1:c.3947C>G	NP_001171914.1:p.Thr1316Ser
NM_001184985.2:c.3947C>G	NP_001171914.1:p.Thr1316Ser
NM_014823.2:c.2426C>G	NP_055638.2:p.Thr809Ser
NM_014823.3:c.2426C>G	NP_055638.2:p.Thr809Ser
NM_018979.3:c.3167C>G	NP_061852.3:p.Thr1056Ser
NM_213655.4:c.3923C>G	NP_998820.3:p.Thr1308Ser
ENST00000315939.10:c.3167C>G	ENSP00000313059.6:p.Thr1056Ser
ENST00000340908.8:c.3923C>G	ENSP00000341292.5:p.Thr1308Ser
ENST00000530271.6:c.4406C>G	ENSP00000433548.3:p.Thr1469Ser
ENST00000535572.5:c.2426C>G	ENSP00000441972.1:p.Thr809Ser
ENST00000537687.5:c.3947C>G	ENSP00000444465.1:p.Thr1316Ser
ENST00000542543.1:n.403C>G
ENST00000544965.5:c.396C>G
ENST00000545055.1:n.277C>G
ENST00000674810.1:n.3764C>G
ENST00000675236.1:n.2062C>G
ENST00000675631.1:c.1946C>G	ENSP00000502415.1:p.Thr649Ser
ENST00000676347.1:c.614C>G	ENSP00000501875.1:p.Thr205Ser
XM_006719003.1:c.3164C>G	XP_006719066.1:p.Thr1055Ser
XM_006719003.2:c.3164C>G	XP_006719066.1:p.Thr1055Ser
XM_011520997.1:c.4406C>G	XP_011519299.1:p.Thr1469Ser
XM_011520997.3:c.4406C>G	XP_011519299.1:p.Thr1469Ser
XM_011520998.1:c.4403C>G	XP_011519300.1:p.Thr1468Ser
XM_011520998.2:c.4403C>G	XP_011519300.1:p.Thr1468Ser
XM_011520999.1:c.4406C>G	XP_011519301.1:p.Thr1469Ser
XM_011520999.2:c.4406C>G	XP_011519301.1:p.Thr1469Ser
XM_011521000.1:c.4406C>G	XP_011519302.1:p.Thr1469Ser
XM_011521000.2:c.4406C>G	XP_011519302.1:p.Thr1469Ser
XM_011521001.1:c.4127C>G	XP_011519303.1:p.Thr1376Ser
XM_011521001.2:c.4127C>G	XP_011519303.1:p.Thr1376Ser
XM_011521002.1:c.3944C>G	XP_011519304.1:p.Thr1315Ser
XM_011521002.2:c.3944C>G	XP_011519304.1:p.Thr1315Ser
XM_011521003.1:c.3668C>G	XP_011519305.1:p.Thr1223Ser
XM_011521003.2:c.3668C>G	XP_011519305.1:p.Thr1223Ser
XM_011521004.1:c.3665C>G	XP_011519306.1:p.Thr1222Ser
XM_011521004.2:c.3665C>G	XP_011519306.1:p.Thr1222Ser
XM_011521005.1:c.3185C>G	XP_011519307.1:p.Thr1062Ser
XM_011521005.2:c.3185C>G	XP_011519307.1:p.Thr1062Ser
XM_011521006.1:c.3083C>G	XP_011519308.1:p.Thr1028Ser
XM_011521006.2:c.3083C>G	XP_011519308.1:p.Thr1028Ser
XM_011521007.1:c.3080C>G	XP_011519309.1:p.Thr1027Ser
XM_011521007.2:c.3080C>G	XP_011519309.1:p.Thr1027Ser
XM_011521008.1:c.2345C>G	XP_011519310.1:p.Thr782Ser
XM_011521008.2:c.2345C>G	XP_011519310.1:p.Thr782Ser
XM_011521009.1:c.2342C>G	XP_011519311.1:p.Thr781Ser
XM_011521009.2:c.2342C>G	XP_011519311.1:p.Thr781Ser
XM_017019834.1:c.2705C>G	XP_016875323.1:p.Thr902Ser
XM_017019835.1:c.2624C>G	XP_016875324.1:p.Thr875Ser
XM_017019836.1:c.2621C>G	XP_016875325.1:p.Thr874Ser
XM_017019837.1:c.2429C>G	XP_016875326.1:p.Thr810Ser
XM_017019838.1:c.2426C>G	XP_016875327.1:p.Thr809Ser
XM_017019839.1:c.2345C>G	XP_016875328.1:p.Thr782Ser