Canonical Allele Identifier: CA2011734403
Community Standard Title: NM_018979.4(WNK1):c.5424G= (p.Met1808=)
Gene: WNK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.889199G= , CM000674.2:g.889199G= GRCh38
NC_000012.11:g.998365G= , CM000674.1:g.998365G= GRCh37
NC_000012.10:g.868626G= NCBI36
NG_007984.2:g.141141G=
NG_007984.3:g.141141G=

Transcript Alleles

HGVS Amino-acid Change
NM_018979.4:c.5424G= MANE Select NP_061852.3:p.Met1808=
ENST00000315939.11:c.5424G= MANE Select ENSP00000313059.6:p.Met1808=
NM_213655.5:c.6180G= MANE Plus Clinical NP_998820.3:p.Met2060=
ENST00000340908.9:c.6180G= MANE Plus Clinical ENSP00000341292.5:p.Met2060=
NM_001184985.1:c.6204G= NP_001171914.1:p.Met2068=
NM_001184985.2:c.6204G= NP_001171914.1:p.Met2068=
NM_014823.2:c.4683G= NP_055638.2:p.Met1561=
NM_014823.3:c.4683G= NP_055638.2:p.Met1561=
NM_018979.3:c.5424G= NP_061852.3:p.Met1808=
NM_213655.4:c.6180G= NP_998820.3:p.Met2060=
ENST00000315939.10:c.5424G= ENSP00000313059.6:p.Met1808=
ENST00000340908.8:c.6180G= ENSP00000341292.5:p.Met2060=
ENST00000530271.6:c.6663G= ENSP00000433548.3:p.Met2221=
ENST00000535572.5:c.4683G= ENSP00000441972.1:p.Met1561=
ENST00000537687.5:c.6204G= ENSP00000444465.1:p.Met2068=
ENST00000675631.1:c.4203G= ENSP00000502415.1:p.Met1401=
ENST00000676347.1:c.2871G= ENSP00000501875.1:p.Met957=
XM_006719003.1:c.5421G= XP_006719066.1:p.Met1807=
XM_006719003.2:c.5421G= XP_006719066.1:p.Met1807=
XM_011520997.1:c.6663G= XP_011519299.1:p.Met2221=
XM_011520997.3:c.6663G= XP_011519299.1:p.Met2221=
XM_011520998.1:c.6660G= XP_011519300.1:p.Met2220=
XM_011520998.2:c.6660G= XP_011519300.1:p.Met2220=
XM_011520999.1:c.6663G= XP_011519301.1:p.Met2221=
XM_011520999.2:c.6663G= XP_011519301.1:p.Met2221=
XM_011521000.1:c.6663G= XP_011519302.1:p.Met2221=
XM_011521000.2:c.6663G= XP_011519302.1:p.Met2221=
XM_011521001.1:c.6384G= XP_011519303.1:p.Met2128=
XM_011521001.2:c.6384G= XP_011519303.1:p.Met2128=
XM_011521002.1:c.6201G= XP_011519304.1:p.Met2067=
XM_011521002.2:c.6201G= XP_011519304.1:p.Met2067=
XM_011521003.1:c.5925G= XP_011519305.1:p.Met1975=
XM_011521003.2:c.5925G= XP_011519305.1:p.Met1975=
XM_011521004.1:c.5922G= XP_011519306.1:p.Met1974=
XM_011521004.2:c.5922G= XP_011519306.1:p.Met1974=
XM_011521005.1:c.5442G= XP_011519307.1:p.Met1814=
XM_011521005.2:c.5442G= XP_011519307.1:p.Met1814=
XM_011521006.1:c.5340G= XP_011519308.1:p.Met1780=
XM_011521006.2:c.5340G= XP_011519308.1:p.Met1780=
XM_011521007.1:c.5337G= XP_011519309.1:p.Met1779=
XM_011521007.2:c.5337G= XP_011519309.1:p.Met1779=
XM_011521008.1:c.4602G= XP_011519310.1:p.Met1534=
XM_011521008.2:c.4602G= XP_011519310.1:p.Met1534=
XM_011521009.1:c.4599G= XP_011519311.1:p.Met1533=
XM_011521009.2:c.4599G= XP_011519311.1:p.Met1533=
XM_017019834.1:c.4962G= XP_016875323.1:p.Met1654=
XM_017019835.1:c.4881G= XP_016875324.1:p.Met1627=
XM_017019836.1:c.4878G= XP_016875325.1:p.Met1626=
XM_017019837.1:c.4686G= XP_016875326.1:p.Met1562=
XM_017019838.1:c.4683G= XP_016875327.1:p.Met1561=
XM_017019839.1:c.4602G= XP_016875328.1:p.Met1534=