Canonical Allele Identifier: CA383333700

Gene: WNK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.857250G>A , CM000674.2:g.857250G>A	GRCh38
NC_000012.11:g.966416G>A , CM000674.1:g.966416G>A	GRCh37
NC_000012.10:g.836677G>A	NCBI36
NG_007984.2:g.109192G>A
NG_007984.3:g.109192G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018979.4:c.1400+1G>A MANE Select	NP_061852.3:n.1400+1G>A
ENST00000315939.11:c.1400+1G>A MANE Select	ENSP00000313059.6:n.1400+1G>A
NM_213655.5:c.1400+1G>A MANE Plus Clinical	NP_998820.3:n.1400+1G>A
ENST00000340908.9:c.1400+1G>A MANE Plus Clinical	ENSP00000341292.5:n.1400+1G>A
NM_001184985.1:c.1400+1G>A	NP_001171914.1:n.1400+1G>A
NM_001184985.2:c.1400+1G>A	NP_001171914.1:n.1400+1G>A
NM_014823.2:c.1400+1G>A	NP_055638.2:n.1400+1G>A
NM_014823.3:c.1400+1G>A	NP_055638.2:n.1400+1G>A
NM_018979.3:c.1400+1G>A	NP_061852.3:n.1400+1G>A
NM_213655.4:c.1400+1G>A	NP_998820.3:n.1400+1G>A
ENST00000315939.10:c.1400+1G>A	ENSP00000313059.6:n.1400+1G>A
ENST00000340908.8:c.1400+1G>A	ENSP00000341292.5:n.1400+1G>A
ENST00000530271.6:c.1400+1G>A	ENSP00000433548.3:n.1400+1G>A
ENST00000535572.5:c.1400+1G>A	ENSP00000441972.1:n.1400+1G>A
ENST00000537687.5:c.1400+1G>A	ENSP00000444465.1:n.1400+1G>A
ENST00000538787.1:n.448+1G>A
ENST00000540360.5:n.325+1G>A
ENST00000675631.1:c.179+1G>A	ENSP00000502415.1:n.179+1G>A
XM_006719003.1:c.1400+1G>A	XP_006719066.1:n.1400+1G>A
XM_006719003.2:c.1400+1G>A	XP_006719066.1:n.1400+1G>A
XM_011520997.1:c.1400+1G>A	XP_011519299.1:n.1400+1G>A
XM_011520997.3:c.1400+1G>A	XP_011519299.1:n.1400+1G>A
XM_011520998.1:c.1400+1G>A	XP_011519300.1:n.1400+1G>A
XM_011520998.2:c.1400+1G>A	XP_011519300.1:n.1400+1G>A
XM_011520999.1:c.1400+1G>A	XP_011519301.1:n.1400+1G>A
XM_011520999.2:c.1400+1G>A	XP_011519301.1:n.1400+1G>A
XM_011521000.1:c.1400+1G>A	XP_011519302.1:n.1400+1G>A
XM_011521000.2:c.1400+1G>A	XP_011519302.1:n.1400+1G>A
XM_011521001.1:c.1400+1G>A	XP_011519303.1:n.1400+1G>A
XM_011521001.2:c.1400+1G>A	XP_011519303.1:n.1400+1G>A
XM_011521002.1:c.1400+1G>A	XP_011519304.1:n.1400+1G>A
XM_011521002.2:c.1400+1G>A	XP_011519304.1:n.1400+1G>A
XM_011521003.1:c.1400+1G>A	XP_011519305.1:n.1400+1G>A
XM_011521003.2:c.1400+1G>A	XP_011519305.1:n.1400+1G>A
XM_011521004.1:c.1400+1G>A	XP_011519306.1:n.1400+1G>A
XM_011521004.2:c.1400+1G>A	XP_011519306.1:n.1400+1G>A
XM_011521005.1:c.179+1G>A	XP_011519307.1:n.179+1G>A
XM_011521005.2:c.179+1G>A	XP_011519307.1:n.179+1G>A
XM_011521006.1:c.1400+1G>A	XP_011519308.1:n.1400+1G>A
XM_011521006.2:c.1400+1G>A	XP_011519308.1:n.1400+1G>A
XM_011521007.1:c.1400+1G>A	XP_011519309.1:n.1400+1G>A
XM_011521007.2:c.1400+1G>A	XP_011519309.1:n.1400+1G>A
XM_011521008.1:c.1400+1G>A	XP_011519310.1:n.1400+1G>A
XM_011521008.2:c.1400+1G>A	XP_011519310.1:n.1400+1G>A
XM_011521009.1:c.1400+1G>A	XP_011519311.1:n.1400+1G>A
XM_011521009.2:c.1400+1G>A	XP_011519311.1:n.1400+1G>A
XM_017019834.1:c.1400+1G>A	XP_016875323.1:n.1400+1G>A
XM_017019835.1:c.1400+1G>A	XP_016875324.1:n.1400+1G>A
XM_017019836.1:c.1400+1G>A	XP_016875325.1:n.1400+1G>A
XM_017019837.1:c.1400+1G>A	XP_016875326.1:n.1400+1G>A
XM_017019838.1:c.1400+1G>A	XP_016875327.1:n.1400+1G>A
XM_017019839.1:c.1400+1G>A	XP_016875328.1:n.1400+1G>A