Canonical Allele Identifier: CA6383037

Gene: WNK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.885627C>T , CM000674.2:g.885627C>T	GRCh38
NC_000012.11:g.994793C>T , CM000674.1:g.994793C>T	GRCh37
NC_000012.10:g.865054C>T	NCBI36
NG_007984.2:g.137569C>T
NG_007984.3:g.137569C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018979.4:c.4823C>T MANE Select	NP_061852.3:p.Ala1608Val
ENST00000315939.11:c.4823C>T MANE Select	ENSP00000313059.6:p.Ala1608Val
NM_213655.5:c.5579C>T MANE Plus Clinical	NP_998820.3:p.Ala1860Val
ENST00000340908.9:c.5579C>T MANE Plus Clinical	ENSP00000341292.5:p.Ala1860Val
NM_001184985.1:c.5603C>T	NP_001171914.1:p.Ala1868Val
NM_001184985.2:c.5603C>T	NP_001171914.1:p.Ala1868Val
NM_014823.2:c.4082C>T	NP_055638.2:p.Ala1361Val
NM_014823.3:c.4082C>T	NP_055638.2:p.Ala1361Val
NM_018979.3:c.4823C>T	NP_061852.3:p.Ala1608Val
NM_213655.4:c.5579C>T	NP_998820.3:p.Ala1860Val
ENST00000315939.10:c.4823C>T	ENSP00000313059.6:p.Ala1608Val
ENST00000340908.8:c.5579C>T	ENSP00000341292.5:p.Ala1860Val
ENST00000530271.6:c.6062C>T	ENSP00000433548.3:p.Ala2021Val
ENST00000535572.5:c.4082C>T	ENSP00000441972.1:p.Ala1361Val
ENST00000537687.5:c.5603C>T	ENSP00000444465.1:p.Ala1868Val
ENST00000675236.1:n.3718C>T
ENST00000675631.1:c.3602C>T	ENSP00000502415.1:p.Ala1201Val
ENST00000676347.1:c.2270C>T	ENSP00000501875.1:p.Ala757Val
XM_006719003.1:c.4820C>T	XP_006719066.1:p.Ala1607Val
XM_006719003.2:c.4820C>T	XP_006719066.1:p.Ala1607Val
XM_011520997.1:c.6062C>T	XP_011519299.1:p.Ala2021Val
XM_011520997.3:c.6062C>T	XP_011519299.1:p.Ala2021Val
XM_011520998.1:c.6059C>T	XP_011519300.1:p.Ala2020Val
XM_011520998.2:c.6059C>T	XP_011519300.1:p.Ala2020Val
XM_011520999.1:c.6062C>T	XP_011519301.1:p.Ala2021Val
XM_011520999.2:c.6062C>T	XP_011519301.1:p.Ala2021Val
XM_011521000.1:c.6062C>T	XP_011519302.1:p.Ala2021Val
XM_011521000.2:c.6062C>T	XP_011519302.1:p.Ala2021Val
XM_011521001.1:c.5783C>T	XP_011519303.1:p.Ala1928Val
XM_011521001.2:c.5783C>T	XP_011519303.1:p.Ala1928Val
XM_011521002.1:c.5600C>T	XP_011519304.1:p.Ala1867Val
XM_011521002.2:c.5600C>T	XP_011519304.1:p.Ala1867Val
XM_011521003.1:c.5324C>T	XP_011519305.1:p.Ala1775Val
XM_011521003.2:c.5324C>T	XP_011519305.1:p.Ala1775Val
XM_011521004.1:c.5321C>T	XP_011519306.1:p.Ala1774Val
XM_011521004.2:c.5321C>T	XP_011519306.1:p.Ala1774Val
XM_011521005.1:c.4841C>T	XP_011519307.1:p.Ala1614Val
XM_011521005.2:c.4841C>T	XP_011519307.1:p.Ala1614Val
XM_011521006.1:c.4739C>T	XP_011519308.1:p.Ala1580Val
XM_011521006.2:c.4739C>T	XP_011519308.1:p.Ala1580Val
XM_011521007.1:c.4736C>T	XP_011519309.1:p.Ala1579Val
XM_011521007.2:c.4736C>T	XP_011519309.1:p.Ala1579Val
XM_011521008.1:c.4001C>T	XP_011519310.1:p.Ala1334Val
XM_011521008.2:c.4001C>T	XP_011519310.1:p.Ala1334Val
XM_011521009.1:c.3998C>T	XP_011519311.1:p.Ala1333Val
XM_011521009.2:c.3998C>T	XP_011519311.1:p.Ala1333Val
XM_017019834.1:c.4361C>T	XP_016875323.1:p.Ala1454Val
XM_017019835.1:c.4280C>T	XP_016875324.1:p.Ala1427Val
XM_017019836.1:c.4277C>T	XP_016875325.1:p.Ala1426Val
XM_017019837.1:c.4085C>T	XP_016875326.1:p.Ala1362Val
XM_017019838.1:c.4082C>T	XP_016875327.1:p.Ala1361Val
XM_017019839.1:c.4001C>T	XP_016875328.1:p.Ala1334Val