Canonical Allele Identifier: CA383334332

Gene: WNK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.894624G>A , CM000674.2:g.894624G>A	GRCh38
NC_000012.11:g.1003790G>A , CM000674.1:g.1003790G>A	GRCh37
NC_000012.10:g.874051G>A	NCBI36
NG_007984.2:g.146566G>A
NG_007984.3:g.146566G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018979.4:c.5572G>A MANE Select	NP_061852.3:p.Gly1858Arg
ENST00000315939.11:c.5572G>A MANE Select	ENSP00000313059.6:p.Gly1858Arg
NM_213655.5:c.6328G>A MANE Plus Clinical	NP_998820.3:p.Gly2110Arg
ENST00000340908.9:c.6328G>A MANE Plus Clinical	ENSP00000341292.5:p.Gly2110Arg
NM_001184985.1:c.6352G>A	NP_001171914.1:p.Gly2118Arg
NM_001184985.2:c.6352G>A	NP_001171914.1:p.Gly2118Arg
NM_014823.2:c.4828G>A	NP_055638.2:p.Gly1610Arg
NM_014823.3:c.4828G>A	NP_055638.2:p.Gly1610Arg
NM_018979.3:c.5572G>A	NP_061852.3:p.Gly1858Arg
NM_213655.4:c.6328G>A	NP_998820.3:p.Gly2110Arg
ENST00000315939.10:c.5572G>A	ENSP00000313059.6:p.Gly1858Arg
ENST00000340908.8:c.6328G>A	ENSP00000341292.5:p.Gly2110Arg
ENST00000530271.6:c.6811G>A	ENSP00000433548.3:p.Gly2271Arg
ENST00000535572.5:c.4828G>A	ENSP00000441972.1:p.Gly1610Arg
ENST00000537687.5:c.6352G>A	ENSP00000444465.1:p.Gly2118Arg
ENST00000675631.1:c.4351G>A	ENSP00000502415.1:p.Gly1451Arg
ENST00000676347.1:c.3019G>A	ENSP00000501875.1:p.Gly1007Arg
XM_006719003.1:c.5569G>A	XP_006719066.1:p.Gly1857Arg
XM_006719003.2:c.5569G>A	XP_006719066.1:p.Gly1857Arg
XM_011520997.1:c.6811G>A	XP_011519299.1:p.Gly2271Arg
XM_011520997.3:c.6811G>A	XP_011519299.1:p.Gly2271Arg
XM_011520998.1:c.6808G>A	XP_011519300.1:p.Gly2270Arg
XM_011520998.2:c.6808G>A	XP_011519300.1:p.Gly2270Arg
XM_011520999.1:c.6808G>A	XP_011519301.1:p.Gly2270Arg
XM_011520999.2:c.6808G>A	XP_011519301.1:p.Gly2270Arg
XM_011521000.1:c.6811G>A	XP_011519302.1:p.Gly2271Arg
XM_011521000.2:c.6811G>A	XP_011519302.1:p.Gly2271Arg
XM_011521001.1:c.6532G>A	XP_011519303.1:p.Gly2178Arg
XM_011521001.2:c.6532G>A	XP_011519303.1:p.Gly2178Arg
XM_011521002.1:c.6349G>A	XP_011519304.1:p.Gly2117Arg
XM_011521002.2:c.6349G>A	XP_011519304.1:p.Gly2117Arg
XM_011521003.1:c.6073G>A	XP_011519305.1:p.Gly2025Arg
XM_011521003.2:c.6073G>A	XP_011519305.1:p.Gly2025Arg
XM_011521004.1:c.6070G>A	XP_011519306.1:p.Gly2024Arg
XM_011521004.2:c.6070G>A	XP_011519306.1:p.Gly2024Arg
XM_011521005.1:c.5590G>A	XP_011519307.1:p.Gly1864Arg
XM_011521005.2:c.5590G>A	XP_011519307.1:p.Gly1864Arg
XM_011521006.1:c.5488G>A	XP_011519308.1:p.Gly1830Arg
XM_011521006.2:c.5488G>A	XP_011519308.1:p.Gly1830Arg
XM_011521007.1:c.5485G>A	XP_011519309.1:p.Gly1829Arg
XM_011521007.2:c.5485G>A	XP_011519309.1:p.Gly1829Arg
XM_011521008.1:c.4750G>A	XP_011519310.1:p.Gly1584Arg
XM_011521008.2:c.4750G>A	XP_011519310.1:p.Gly1584Arg
XM_011521009.1:c.4747G>A	XP_011519311.1:p.Gly1583Arg
XM_011521009.2:c.4747G>A	XP_011519311.1:p.Gly1583Arg
XM_017019834.1:c.5110G>A	XP_016875323.1:p.Gly1704Arg
XM_017019835.1:c.5029G>A	XP_016875324.1:p.Gly1677Arg
XM_017019836.1:c.5026G>A	XP_016875325.1:p.Gly1676Arg
XM_017019837.1:c.4834G>A	XP_016875326.1:p.Gly1612Arg
XM_017019838.1:c.4831G>A	XP_016875327.1:p.Gly1611Arg
XM_017019839.1:c.4750G>A	XP_016875328.1:p.Gly1584Arg