Canonical Allele Identifier: CA6382646

Gene: WNK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.880990A>G , CM000674.2:g.880990A>G	GRCh38
NC_000012.11:g.990156A>G , CM000674.1:g.990156A>G	GRCh37
NC_000012.10:g.860417A>G	NCBI36
NG_007984.2:g.132932A>G
NG_007984.3:g.132932A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018979.4:c.3102A>G MANE Select	NP_061852.3:p.Ala1034=
ENST00000315939.11:c.3102A>G MANE Select	ENSP00000313059.6:p.Ala1034=
NM_213655.5:c.3868-702A>G MANE Plus Clinical	NP_998820.3:n.3868-702A>G
ENST00000340908.9:c.3868-702A>G MANE Plus Clinical	ENSP00000341292.5:n.3868-702A>G
NM_001184985.1:c.3882A>G	NP_001171914.1:p.Ala1294=
NM_001184985.2:c.3882A>G	NP_001171914.1:p.Ala1294=
NM_014823.2:c.2371-702A>G	NP_055638.2:n.2371-702A>G
NM_014823.3:c.2371-702A>G	NP_055638.2:n.2371-702A>G
NM_018979.3:c.3102A>G	NP_061852.3:p.Ala1034=
NM_213655.4:c.3868-702A>G	NP_998820.3:n.3868-702A>G
ENST00000315939.10:c.3102A>G	ENSP00000313059.6:p.Ala1034=
ENST00000340908.8:c.3868-702A>G	ENSP00000341292.5:n.3868-702A>G
ENST00000530271.6:c.4341A>G	ENSP00000433548.3:p.Ala1447=
ENST00000535572.5:c.2371-702A>G	ENSP00000441972.1:n.2371-702A>G
ENST00000537687.5:c.3882A>G	ENSP00000444465.1:p.Ala1294=
ENST00000542543.1:n.348-702A>G
ENST00000544965.5:c.341-702A>G
ENST00000674810.1:n.3699A>G
ENST00000675236.1:n.1997A>G
ENST00000675631.1:c.1881A>G	ENSP00000502415.1:p.Ala627=
ENST00000676347.1:c.559-702A>G	ENSP00000501875.1:n.559-702A>G
XM_006719003.1:c.3099A>G	XP_006719066.1:p.Ala1033=
XM_006719003.2:c.3099A>G	XP_006719066.1:p.Ala1033=
XM_011520997.1:c.4341A>G	XP_011519299.1:p.Ala1447=
XM_011520997.3:c.4341A>G	XP_011519299.1:p.Ala1447=
XM_011520998.1:c.4338A>G	XP_011519300.1:p.Ala1446=
XM_011520998.2:c.4338A>G	XP_011519300.1:p.Ala1446=
XM_011520999.1:c.4341A>G	XP_011519301.1:p.Ala1447=
XM_011520999.2:c.4341A>G	XP_011519301.1:p.Ala1447=
XM_011521000.1:c.4341A>G	XP_011519302.1:p.Ala1447=
XM_011521000.2:c.4341A>G	XP_011519302.1:p.Ala1447=
XM_011521001.1:c.4072-702A>G	XP_011519303.1:n.4072-702A>G
XM_011521001.2:c.4072-702A>G	XP_011519303.1:n.4072-702A>G
XM_011521002.1:c.3879A>G	XP_011519304.1:p.Ala1293=
XM_011521002.2:c.3879A>G	XP_011519304.1:p.Ala1293=
XM_011521003.1:c.3613-702A>G	XP_011519305.1:n.3613-702A>G
XM_011521003.2:c.3613-702A>G	XP_011519305.1:n.3613-702A>G
XM_011521004.1:c.3610-702A>G	XP_011519306.1:n.3610-702A>G
XM_011521004.2:c.3610-702A>G	XP_011519306.1:n.3610-702A>G
XM_011521005.1:c.3120A>G	XP_011519307.1:p.Ala1040=
XM_011521005.2:c.3120A>G	XP_011519307.1:p.Ala1040=
XM_011521006.1:c.3018A>G	XP_011519308.1:p.Ala1006=
XM_011521006.2:c.3018A>G	XP_011519308.1:p.Ala1006=
XM_011521007.1:c.3015A>G	XP_011519309.1:p.Ala1005=
XM_011521007.2:c.3015A>G	XP_011519309.1:p.Ala1005=
XM_011521008.1:c.2290-702A>G	XP_011519310.1:n.2290-702A>G
XM_011521008.2:c.2290-702A>G	XP_011519310.1:n.2290-702A>G
XM_011521009.1:c.2287-702A>G	XP_011519311.1:n.2287-702A>G
XM_011521009.2:c.2287-702A>G	XP_011519311.1:n.2287-702A>G
XM_017019834.1:c.2640A>G	XP_016875323.1:p.Ala880=
XM_017019835.1:c.2559A>G	XP_016875324.1:p.Ala853=
XM_017019836.1:c.2556A>G	XP_016875325.1:p.Ala852=
XM_017019837.1:c.2374-702A>G	XP_016875326.1:n.2374-702A>G
XM_017019838.1:c.2371-702A>G	XP_016875327.1:n.2371-702A>G
XM_017019839.1:c.2290-702A>G	XP_016875328.1:n.2290-702A>G