Canonical Allele Identifier: CA6382918

Gene: WNK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.884908A>G , CM000674.2:g.884908A>G	GRCh38
NC_000012.11:g.994074A>G , CM000674.1:g.994074A>G	GRCh37
NC_000012.10:g.864335A>G	NCBI36
NG_007984.2:g.136850A>G
NG_007984.3:g.136850A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018979.4:c.4104A>G MANE Select	NP_061852.3:p.Thr1368=
ENST00000315939.11:c.4104A>G MANE Select	ENSP00000313059.6:p.Thr1368=
NM_213655.5:c.4860A>G MANE Plus Clinical	NP_998820.3:p.Thr1620=
ENST00000340908.9:c.4860A>G MANE Plus Clinical	ENSP00000341292.5:p.Thr1620=
NM_001184985.1:c.4884A>G	NP_001171914.1:p.Thr1628=
NM_001184985.2:c.4884A>G	NP_001171914.1:p.Thr1628=
NM_014823.2:c.3363A>G	NP_055638.2:p.Thr1121=
NM_014823.3:c.3363A>G	NP_055638.2:p.Thr1121=
NM_018979.3:c.4104A>G	NP_061852.3:p.Thr1368=
NM_213655.4:c.4860A>G	NP_998820.3:p.Thr1620=
ENST00000315939.10:c.4104A>G	ENSP00000313059.6:p.Thr1368=
ENST00000340908.8:c.4860A>G	ENSP00000341292.5:p.Thr1620=
ENST00000530271.6:c.5343A>G	ENSP00000433548.3:p.Thr1781=
ENST00000535572.5:c.3363A>G	ENSP00000441972.1:p.Thr1121=
ENST00000537687.5:c.4884A>G	ENSP00000444465.1:p.Thr1628=
ENST00000674810.1:n.4701A>G
ENST00000675236.1:n.2999A>G
ENST00000675631.1:c.2883A>G	ENSP00000502415.1:p.Thr961=
ENST00000676347.1:c.1551A>G	ENSP00000501875.1:p.Thr517=
XM_006719003.1:c.4101A>G	XP_006719066.1:p.Thr1367=
XM_006719003.2:c.4101A>G	XP_006719066.1:p.Thr1367=
XM_011520997.1:c.5343A>G	XP_011519299.1:p.Thr1781=
XM_011520997.3:c.5343A>G	XP_011519299.1:p.Thr1781=
XM_011520998.1:c.5340A>G	XP_011519300.1:p.Thr1780=
XM_011520998.2:c.5340A>G	XP_011519300.1:p.Thr1780=
XM_011520999.1:c.5343A>G	XP_011519301.1:p.Thr1781=
XM_011520999.2:c.5343A>G	XP_011519301.1:p.Thr1781=
XM_011521000.1:c.5343A>G	XP_011519302.1:p.Thr1781=
XM_011521000.2:c.5343A>G	XP_011519302.1:p.Thr1781=
XM_011521001.1:c.5064A>G	XP_011519303.1:p.Thr1688=
XM_011521001.2:c.5064A>G	XP_011519303.1:p.Thr1688=
XM_011521002.1:c.4881A>G	XP_011519304.1:p.Thr1627=
XM_011521002.2:c.4881A>G	XP_011519304.1:p.Thr1627=
XM_011521003.1:c.4605A>G	XP_011519305.1:p.Thr1535=
XM_011521003.2:c.4605A>G	XP_011519305.1:p.Thr1535=
XM_011521004.1:c.4602A>G	XP_011519306.1:p.Thr1534=
XM_011521004.2:c.4602A>G	XP_011519306.1:p.Thr1534=
XM_011521005.1:c.4122A>G	XP_011519307.1:p.Thr1374=
XM_011521005.2:c.4122A>G	XP_011519307.1:p.Thr1374=
XM_011521006.1:c.4020A>G	XP_011519308.1:p.Thr1340=
XM_011521006.2:c.4020A>G	XP_011519308.1:p.Thr1340=
XM_011521007.1:c.4017A>G	XP_011519309.1:p.Thr1339=
XM_011521007.2:c.4017A>G	XP_011519309.1:p.Thr1339=
XM_011521008.1:c.3282A>G	XP_011519310.1:p.Thr1094=
XM_011521008.2:c.3282A>G	XP_011519310.1:p.Thr1094=
XM_011521009.1:c.3279A>G	XP_011519311.1:p.Thr1093=
XM_011521009.2:c.3279A>G	XP_011519311.1:p.Thr1093=
XM_017019834.1:c.3642A>G	XP_016875323.1:p.Thr1214=
XM_017019835.1:c.3561A>G	XP_016875324.1:p.Thr1187=
XM_017019836.1:c.3558A>G	XP_016875325.1:p.Thr1186=
XM_017019837.1:c.3366A>G	XP_016875326.1:p.Thr1122=
XM_017019838.1:c.3363A>G	XP_016875327.1:p.Thr1121=
XM_017019839.1:c.3282A>G	XP_016875328.1:p.Thr1094=