Canonical Allele Identifier: CA6383293
Community Standard Title: NM_018979.4(WNK1):c.5851A>G (p.Thr1951Ala)
Gene: WNK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.896338A>G , CM000674.2:g.896338A>G GRCh38
NC_000012.11:g.1005504A>G , CM000674.1:g.1005504A>G GRCh37
NC_000012.10:g.875765A>G NCBI36
NG_007984.2:g.148280A>G
NG_007984.3:g.148280A>G

Transcript Alleles

HGVS Amino-acid Change
NM_018979.4:c.5851A>G MANE Select NP_061852.3:p.Thr1951Ala
ENST00000315939.11:c.5851A>G MANE Select ENSP00000313059.6:p.Thr1951Ala
NM_213655.5:c.6607A>G MANE Plus Clinical NP_998820.3:p.Thr2203Ala
ENST00000340908.9:c.6607A>G MANE Plus Clinical ENSP00000341292.5:p.Thr2203Ala
NM_001184985.1:c.6631A>G NP_001171914.1:p.Thr2211Ala
NM_001184985.2:c.6631A>G NP_001171914.1:p.Thr2211Ala
NM_014823.2:c.5107A>G NP_055638.2:p.Thr1703Ala
NM_014823.3:c.5107A>G NP_055638.2:p.Thr1703Ala
NM_018979.3:c.5851A>G NP_061852.3:p.Thr1951Ala
NM_213655.4:c.6607A>G NP_998820.3:p.Thr2203Ala
ENST00000315939.10:c.5851A>G ENSP00000313059.6:p.Thr1951Ala
ENST00000340908.8:c.6607A>G ENSP00000341292.5:p.Thr2203Ala
ENST00000530271.6:c.7090A>G ENSP00000433548.3:p.Thr2364Ala
ENST00000535572.5:c.5107A>G ENSP00000441972.1:p.Thr1703Ala
ENST00000537687.5:c.6631A>G ENSP00000444465.1:p.Thr2211Ala
ENST00000675631.1:c.4630A>G ENSP00000502415.1:p.Thr1544Ala
ENST00000676347.1:c.3298A>G ENSP00000501875.1:p.Thr1100Ala
XM_006719003.1:c.5848A>G XP_006719066.1:p.Thr1950Ala
XM_006719003.2:c.5848A>G XP_006719066.1:p.Thr1950Ala
XM_011520997.1:c.7090A>G XP_011519299.1:p.Thr2364Ala
XM_011520997.3:c.7090A>G XP_011519299.1:p.Thr2364Ala
XM_011520998.1:c.7087A>G XP_011519300.1:p.Thr2363Ala
XM_011520998.2:c.7087A>G XP_011519300.1:p.Thr2363Ala
XM_011520999.1:c.7087A>G XP_011519301.1:p.Thr2363Ala
XM_011520999.2:c.7087A>G XP_011519301.1:p.Thr2363Ala
XM_011521000.1:c.7090A>G XP_011519302.1:p.Thr2364Ala
XM_011521000.2:c.7090A>G XP_011519302.1:p.Thr2364Ala
XM_011521001.1:c.6811A>G XP_011519303.1:p.Thr2271Ala
XM_011521001.2:c.6811A>G XP_011519303.1:p.Thr2271Ala
XM_011521002.1:c.6628A>G XP_011519304.1:p.Thr2210Ala
XM_011521002.2:c.6628A>G XP_011519304.1:p.Thr2210Ala
XM_011521003.1:c.6352A>G XP_011519305.1:p.Thr2118Ala
XM_011521003.2:c.6352A>G XP_011519305.1:p.Thr2118Ala
XM_011521004.1:c.6349A>G XP_011519306.1:p.Thr2117Ala
XM_011521004.2:c.6349A>G XP_011519306.1:p.Thr2117Ala
XM_011521005.1:c.5869A>G XP_011519307.1:p.Thr1957Ala
XM_011521005.2:c.5869A>G XP_011519307.1:p.Thr1957Ala
XM_011521006.1:c.5767A>G XP_011519308.1:p.Thr1923Ala
XM_011521006.2:c.5767A>G XP_011519308.1:p.Thr1923Ala
XM_011521007.1:c.5764A>G XP_011519309.1:p.Thr1922Ala
XM_011521007.2:c.5764A>G XP_011519309.1:p.Thr1922Ala
XM_011521008.1:c.5029A>G XP_011519310.1:p.Thr1677Ala
XM_011521008.2:c.5029A>G XP_011519310.1:p.Thr1677Ala
XM_011521009.1:c.5026A>G XP_011519311.1:p.Thr1676Ala
XM_011521009.2:c.5026A>G XP_011519311.1:p.Thr1676Ala
XM_017019834.1:c.5389A>G XP_016875323.1:p.Thr1797Ala
XM_017019835.1:c.5308A>G XP_016875324.1:p.Thr1770Ala
XM_017019836.1:c.5305A>G XP_016875325.1:p.Thr1769Ala
XM_017019837.1:c.5113A>G XP_016875326.1:p.Thr1705Ala
XM_017019838.1:c.5110A>G XP_016875327.1:p.Thr1704Ala
XM_017019839.1:c.5029A>G XP_016875328.1:p.Thr1677Ala