Canonical Allele Identifier: CA6383134

Gene: WNK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.887265C>T , CM000674.2:g.887265C>T	GRCh38
NC_000012.11:g.996431C>T , CM000674.1:g.996431C>T	GRCh37
NC_000012.10:g.866692C>T	NCBI36
NG_007984.2:g.139207C>T
NG_007984.3:g.139207C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018979.4:c.5325C>T MANE Select	NP_061852.3:p.Ser1775=
ENST00000315939.11:c.5325C>T MANE Select	ENSP00000313059.6:p.Ser1775=
NM_213655.5:c.6081C>T MANE Plus Clinical	NP_998820.3:p.Ser2027=
ENST00000340908.9:c.6081C>T MANE Plus Clinical	ENSP00000341292.5:p.Ser2027=
NM_001184985.1:c.6105C>T	NP_001171914.1:p.Ser2035=
NM_001184985.2:c.6105C>T	NP_001171914.1:p.Ser2035=
NM_014823.2:c.4584C>T	NP_055638.2:p.Ser1528=
NM_014823.3:c.4584C>T	NP_055638.2:p.Ser1528=
NM_018979.3:c.5325C>T	NP_061852.3:p.Ser1775=
NM_213655.4:c.6081C>T	NP_998820.3:p.Ser2027=
ENST00000315939.10:c.5325C>T	ENSP00000313059.6:p.Ser1775=
ENST00000340908.8:c.6081C>T	ENSP00000341292.5:p.Ser2027=
ENST00000530271.6:c.6564C>T	ENSP00000433548.3:p.Ser2188=
ENST00000535572.5:c.4584C>T	ENSP00000441972.1:p.Ser1528=
ENST00000537687.5:c.6105C>T	ENSP00000444465.1:p.Ser2035=
ENST00000675631.1:c.4104C>T	ENSP00000502415.1:p.Ser1368=
ENST00000676347.1:c.2772C>T	ENSP00000501875.1:p.Ser924=
XM_006719003.1:c.5322C>T	XP_006719066.1:p.Ser1774=
XM_006719003.2:c.5322C>T	XP_006719066.1:p.Ser1774=
XM_011520997.1:c.6564C>T	XP_011519299.1:p.Ser2188=
XM_011520997.3:c.6564C>T	XP_011519299.1:p.Ser2188=
XM_011520998.1:c.6561C>T	XP_011519300.1:p.Ser2187=
XM_011520998.2:c.6561C>T	XP_011519300.1:p.Ser2187=
XM_011520999.1:c.6564C>T	XP_011519301.1:p.Ser2188=
XM_011520999.2:c.6564C>T	XP_011519301.1:p.Ser2188=
XM_011521000.1:c.6564C>T	XP_011519302.1:p.Ser2188=
XM_011521000.2:c.6564C>T	XP_011519302.1:p.Ser2188=
XM_011521001.1:c.6285C>T	XP_011519303.1:p.Ser2095=
XM_011521001.2:c.6285C>T	XP_011519303.1:p.Ser2095=
XM_011521002.1:c.6102C>T	XP_011519304.1:p.Ser2034=
XM_011521002.2:c.6102C>T	XP_011519304.1:p.Ser2034=
XM_011521003.1:c.5826C>T	XP_011519305.1:p.Ser1942=
XM_011521003.2:c.5826C>T	XP_011519305.1:p.Ser1942=
XM_011521004.1:c.5823C>T	XP_011519306.1:p.Ser1941=
XM_011521004.2:c.5823C>T	XP_011519306.1:p.Ser1941=
XM_011521005.1:c.5343C>T	XP_011519307.1:p.Ser1781=
XM_011521005.2:c.5343C>T	XP_011519307.1:p.Ser1781=
XM_011521006.1:c.5241C>T	XP_011519308.1:p.Ser1747=
XM_011521006.2:c.5241C>T	XP_011519308.1:p.Ser1747=
XM_011521007.1:c.5238C>T	XP_011519309.1:p.Ser1746=
XM_011521007.2:c.5238C>T	XP_011519309.1:p.Ser1746=
XM_011521008.1:c.4503C>T	XP_011519310.1:p.Ser1501=
XM_011521008.2:c.4503C>T	XP_011519310.1:p.Ser1501=
XM_011521009.1:c.4500C>T	XP_011519311.1:p.Ser1500=
XM_011521009.2:c.4500C>T	XP_011519311.1:p.Ser1500=
XM_017019834.1:c.4863C>T	XP_016875323.1:p.Ser1621=
XM_017019835.1:c.4782C>T	XP_016875324.1:p.Ser1594=
XM_017019836.1:c.4779C>T	XP_016875325.1:p.Ser1593=
XM_017019837.1:c.4587C>T	XP_016875326.1:p.Ser1529=
XM_017019838.1:c.4584C>T	XP_016875327.1:p.Ser1528=
XM_017019839.1:c.4503C>T	XP_016875328.1:p.Ser1501=