Canonical Allele Identifier: CA6382793
Community Standard Title: NM_018979.4(WNK1):c.3492G>A (p.Val1164=)
Gene: WNK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.883397G>A , CM000674.2:g.883397G>A GRCh38
NC_000012.11:g.992563G>A , CM000674.1:g.992563G>A GRCh37
NC_000012.10:g.862824G>A NCBI36
NG_007984.2:g.135339G>A
NG_007984.3:g.135339G>A

Transcript Alleles

HGVS Amino-acid Change
NM_018979.4:c.3492G>A MANE Select NP_061852.3:p.Val1164=
ENST00000315939.11:c.3492G>A MANE Select ENSP00000313059.6:p.Val1164=
NM_213655.5:c.4248G>A MANE Plus Clinical NP_998820.3:p.Val1416=
ENST00000340908.9:c.4248G>A MANE Plus Clinical ENSP00000341292.5:p.Val1416=
NM_001184985.1:c.4272G>A NP_001171914.1:p.Val1424=
NM_001184985.2:c.4272G>A NP_001171914.1:p.Val1424=
NM_014823.2:c.2751G>A NP_055638.2:p.Val917=
NM_014823.3:c.2751G>A NP_055638.2:p.Val917=
NM_018979.3:c.3492G>A NP_061852.3:p.Val1164=
NM_213655.4:c.4248G>A NP_998820.3:p.Val1416=
ENST00000315939.10:c.3492G>A ENSP00000313059.6:p.Val1164=
ENST00000340908.8:c.4248G>A ENSP00000341292.5:p.Val1416=
ENST00000530271.6:c.4731G>A ENSP00000433548.3:p.Val1577=
ENST00000534872.1:c.192G>A ENSP00000446253.1:p.Val64=
ENST00000535572.5:c.2751G>A ENSP00000441972.1:p.Val917=
ENST00000537687.5:c.4272G>A ENSP00000444465.1:p.Val1424=
ENST00000545055.1:n.602G>A
ENST00000674810.1:n.4089G>A
ENST00000675236.1:n.2387G>A
ENST00000675631.1:c.2271G>A ENSP00000502415.1:p.Val757=
ENST00000676347.1:c.939G>A ENSP00000501875.1:p.Val313=
XM_006719003.1:c.3489G>A XP_006719066.1:p.Val1163=
XM_006719003.2:c.3489G>A XP_006719066.1:p.Val1163=
XM_011520997.1:c.4731G>A XP_011519299.1:p.Val1577=
XM_011520997.3:c.4731G>A XP_011519299.1:p.Val1577=
XM_011520998.1:c.4728G>A XP_011519300.1:p.Val1576=
XM_011520998.2:c.4728G>A XP_011519300.1:p.Val1576=
XM_011520999.1:c.4731G>A XP_011519301.1:p.Val1577=
XM_011520999.2:c.4731G>A XP_011519301.1:p.Val1577=
XM_011521000.1:c.4731G>A XP_011519302.1:p.Val1577=
XM_011521000.2:c.4731G>A XP_011519302.1:p.Val1577=
XM_011521001.1:c.4452G>A XP_011519303.1:p.Val1484=
XM_011521001.2:c.4452G>A XP_011519303.1:p.Val1484=
XM_011521002.1:c.4269G>A XP_011519304.1:p.Val1423=
XM_011521002.2:c.4269G>A XP_011519304.1:p.Val1423=
XM_011521003.1:c.3993G>A XP_011519305.1:p.Val1331=
XM_011521003.2:c.3993G>A XP_011519305.1:p.Val1331=
XM_011521004.1:c.3990G>A XP_011519306.1:p.Val1330=
XM_011521004.2:c.3990G>A XP_011519306.1:p.Val1330=
XM_011521005.1:c.3510G>A XP_011519307.1:p.Val1170=
XM_011521005.2:c.3510G>A XP_011519307.1:p.Val1170=
XM_011521006.1:c.3408G>A XP_011519308.1:p.Val1136=
XM_011521006.2:c.3408G>A XP_011519308.1:p.Val1136=
XM_011521007.1:c.3405G>A XP_011519309.1:p.Val1135=
XM_011521007.2:c.3405G>A XP_011519309.1:p.Val1135=
XM_011521008.1:c.2670G>A XP_011519310.1:p.Val890=
XM_011521008.2:c.2670G>A XP_011519310.1:p.Val890=
XM_011521009.1:c.2667G>A XP_011519311.1:p.Val889=
XM_011521009.2:c.2667G>A XP_011519311.1:p.Val889=
XM_017019834.1:c.3030G>A XP_016875323.1:p.Val1010=
XM_017019835.1:c.2949G>A XP_016875324.1:p.Val983=
XM_017019836.1:c.2946G>A XP_016875325.1:p.Val982=
XM_017019837.1:c.2754G>A XP_016875326.1:p.Val918=
XM_017019838.1:c.2751G>A XP_016875327.1:p.Val917=
XM_017019839.1:c.2670G>A XP_016875328.1:p.Val890=