Canonical Allele Identifier: CA6383269

Gene: WNK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.896201T>A , CM000674.2:g.896201T>A	GRCh38
NC_000012.11:g.1005367T>A , CM000674.1:g.1005367T>A	GRCh37
NC_000012.10:g.875628T>A	NCBI36
NG_007984.2:g.148143T>A
NG_007984.3:g.148143T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018979.4:c.5714T>A MANE Select	NP_061852.3:p.Val1905Glu
ENST00000315939.11:c.5714T>A MANE Select	ENSP00000313059.6:p.Val1905Glu
NM_213655.5:c.6470T>A MANE Plus Clinical	NP_998820.3:p.Val2157Glu
ENST00000340908.9:c.6470T>A MANE Plus Clinical	ENSP00000341292.5:p.Val2157Glu
NM_001184985.1:c.6494T>A	NP_001171914.1:p.Val2165Glu
NM_001184985.2:c.6494T>A	NP_001171914.1:p.Val2165Glu
NM_014823.2:c.4970T>A	NP_055638.2:p.Val1657Glu
NM_014823.3:c.4970T>A	NP_055638.2:p.Val1657Glu
NM_018979.3:c.5714T>A	NP_061852.3:p.Val1905Glu
NM_213655.4:c.6470T>A	NP_998820.3:p.Val2157Glu
ENST00000315939.10:c.5714T>A	ENSP00000313059.6:p.Val1905Glu
ENST00000340908.8:c.6470T>A	ENSP00000341292.5:p.Val2157Glu
ENST00000530271.6:c.6953T>A	ENSP00000433548.3:p.Val2318Glu
ENST00000535572.5:c.4970T>A	ENSP00000441972.1:p.Val1657Glu
ENST00000537687.5:c.6494T>A	ENSP00000444465.1:p.Val2165Glu
ENST00000675631.1:c.4493T>A	ENSP00000502415.1:p.Val1498Glu
ENST00000676347.1:c.3161T>A	ENSP00000501875.1:p.Val1054Glu
XM_006719003.1:c.5711T>A	XP_006719066.1:p.Val1904Glu
XM_006719003.2:c.5711T>A	XP_006719066.1:p.Val1904Glu
XM_011520997.1:c.6953T>A	XP_011519299.1:p.Val2318Glu
XM_011520997.3:c.6953T>A	XP_011519299.1:p.Val2318Glu
XM_011520998.1:c.6950T>A	XP_011519300.1:p.Val2317Glu
XM_011520998.2:c.6950T>A	XP_011519300.1:p.Val2317Glu
XM_011520999.1:c.6950T>A	XP_011519301.1:p.Val2317Glu
XM_011520999.2:c.6950T>A	XP_011519301.1:p.Val2317Glu
XM_011521000.1:c.6953T>A	XP_011519302.1:p.Val2318Glu
XM_011521000.2:c.6953T>A	XP_011519302.1:p.Val2318Glu
XM_011521001.1:c.6674T>A	XP_011519303.1:p.Val2225Glu
XM_011521001.2:c.6674T>A	XP_011519303.1:p.Val2225Glu
XM_011521002.1:c.6491T>A	XP_011519304.1:p.Val2164Glu
XM_011521002.2:c.6491T>A	XP_011519304.1:p.Val2164Glu
XM_011521003.1:c.6215T>A	XP_011519305.1:p.Val2072Glu
XM_011521003.2:c.6215T>A	XP_011519305.1:p.Val2072Glu
XM_011521004.1:c.6212T>A	XP_011519306.1:p.Val2071Glu
XM_011521004.2:c.6212T>A	XP_011519306.1:p.Val2071Glu
XM_011521005.1:c.5732T>A	XP_011519307.1:p.Val1911Glu
XM_011521005.2:c.5732T>A	XP_011519307.1:p.Val1911Glu
XM_011521006.1:c.5630T>A	XP_011519308.1:p.Val1877Glu
XM_011521006.2:c.5630T>A	XP_011519308.1:p.Val1877Glu
XM_011521007.1:c.5627T>A	XP_011519309.1:p.Val1876Glu
XM_011521007.2:c.5627T>A	XP_011519309.1:p.Val1876Glu
XM_011521008.1:c.4892T>A	XP_011519310.1:p.Val1631Glu
XM_011521008.2:c.4892T>A	XP_011519310.1:p.Val1631Glu
XM_011521009.1:c.4889T>A	XP_011519311.1:p.Val1630Glu
XM_011521009.2:c.4889T>A	XP_011519311.1:p.Val1630Glu
XM_017019834.1:c.5252T>A	XP_016875323.1:p.Val1751Glu
XM_017019835.1:c.5171T>A	XP_016875324.1:p.Val1724Glu
XM_017019836.1:c.5168T>A	XP_016875325.1:p.Val1723Glu
XM_017019837.1:c.4976T>A	XP_016875326.1:p.Val1659Glu
XM_017019838.1:c.4973T>A	XP_016875327.1:p.Val1658Glu
XM_017019839.1:c.4892T>A	XP_016875328.1:p.Val1631Glu