Canonical Allele Identifier: CA478084089

Gene: WNK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.885400A>G , CM000674.2:g.885400A>G	GRCh38
NC_000012.11:g.994566A>G , CM000674.1:g.994566A>G	GRCh37
NC_000012.10:g.864827A>G	NCBI36
NG_007984.2:g.137342A>G
NG_007984.3:g.137342A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315939.11:c.4596A>G MANE Select	ENSP00000313059.6:p.Thr1532=
ENST00000340908.9:c.5352A>G MANE Plus Clinical	ENSP00000341292.5:p.Thr1784=
ENST00000675236.1:n.3491A>G
ENST00000675631.1:c.3375A>G	ENSP00000502415.1:p.Thr1125=
ENST00000676347.1:c.2043A>G	ENSP00000501875.1:p.Thr681=
ENST00000315939.10:c.4596A>G	ENSP00000313059.6:p.Thr1532=
ENST00000340908.8:c.5352A>G	ENSP00000341292.5:p.Thr1784=
ENST00000530271.6:c.5835A>G	ENSP00000433548.3:p.Thr1945=
ENST00000535572.5:c.3855A>G	ENSP00000441972.1:p.Thr1285=
ENST00000537687.5:c.5376A>G	ENSP00000444465.1:p.Thr1792=
NM_001184985.1:c.5376A>G	NP_001171914.1:p.Thr1792=
NM_014823.2:c.3855A>G	NP_055638.2:p.Thr1285=
NM_018979.3:c.4596A>G	NP_061852.3:p.Thr1532=
NM_213655.4:c.5352A>G	NP_998820.3:p.Thr1784=
XM_006719003.1:c.4593A>G	XP_006719066.1:p.Thr1531=
XM_011520997.1:c.5835A>G	XP_011519299.1:p.Thr1945=
XM_011520998.1:c.5832A>G	XP_011519300.1:p.Thr1944=
XM_011520999.1:c.5835A>G	XP_011519301.1:p.Thr1945=
XM_011521000.1:c.5835A>G	XP_011519302.1:p.Thr1945=
XM_011521001.1:c.5556A>G	XP_011519303.1:p.Thr1852=
XM_011521002.1:c.5373A>G	XP_011519304.1:p.Thr1791=
XM_011521003.1:c.5097A>G	XP_011519305.1:p.Thr1699=
XM_011521004.1:c.5094A>G	XP_011519306.1:p.Thr1698=
XM_011521005.1:c.4614A>G	XP_011519307.1:p.Thr1538=
XM_011521006.1:c.4512A>G	XP_011519308.1:p.Thr1504=
XM_011521007.1:c.4509A>G	XP_011519309.1:p.Thr1503=
XM_011521008.1:c.3774A>G	XP_011519310.1:p.Thr1258=
XM_011521009.1:c.3771A>G	XP_011519311.1:p.Thr1257=
XM_006719003.2:c.4593A>G	XP_006719066.1:p.Thr1531=
XM_011520997.3:c.5835A>G	XP_011519299.1:p.Thr1945=
XM_011520998.2:c.5832A>G	XP_011519300.1:p.Thr1944=
XM_011520999.2:c.5835A>G	XP_011519301.1:p.Thr1945=
XM_011521000.2:c.5835A>G	XP_011519302.1:p.Thr1945=
XM_011521001.2:c.5556A>G	XP_011519303.1:p.Thr1852=
XM_011521002.2:c.5373A>G	XP_011519304.1:p.Thr1791=
XM_011521003.2:c.5097A>G	XP_011519305.1:p.Thr1699=
XM_011521004.2:c.5094A>G	XP_011519306.1:p.Thr1698=
XM_011521005.2:c.4614A>G	XP_011519307.1:p.Thr1538=
XM_011521006.2:c.4512A>G	XP_011519308.1:p.Thr1504=
XM_011521007.2:c.4509A>G	XP_011519309.1:p.Thr1503=
XM_011521008.2:c.3774A>G	XP_011519310.1:p.Thr1258=
XM_011521009.2:c.3771A>G	XP_011519311.1:p.Thr1257=
XM_017019834.1:c.4134A>G	XP_016875323.1:p.Thr1378=
XM_017019835.1:c.4053A>G	XP_016875324.1:p.Thr1351=
XM_017019836.1:c.4050A>G	XP_016875325.1:p.Thr1350=
XM_017019837.1:c.3858A>G	XP_016875326.1:p.Thr1286=
XM_017019838.1:c.3855A>G	XP_016875327.1:p.Thr1285=
XM_017019839.1:c.3774A>G	XP_016875328.1:p.Thr1258=
NM_018979.4:c.4596A>G MANE Select	NP_061852.3:p.Thr1532=
NM_014823.3:c.3855A>G	NP_055638.2:p.Thr1285=
NM_001184985.2:c.5376A>G	NP_001171914.1:p.Thr1792=
NM_213655.5:c.5352A>G MANE Plus Clinical	NP_998820.3:p.Thr1784=