Canonical Allele Identifier: CA231478997

Gene: WNK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.884795C>T , CM000674.2:g.884795C>T	GRCh38
NC_000012.11:g.993961C>T , CM000674.1:g.993961C>T	GRCh37
NC_000012.10:g.864222C>T	NCBI36
NG_007984.2:g.136737C>T
NG_007984.3:g.136737C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018979.4:c.3991C>T MANE Select	NP_061852.3:p.Pro1331Ser
ENST00000315939.11:c.3991C>T MANE Select	ENSP00000313059.6:p.Pro1331Ser
NM_213655.5:c.4747C>T MANE Plus Clinical	NP_998820.3:p.Pro1583Ser
ENST00000340908.9:c.4747C>T MANE Plus Clinical	ENSP00000341292.5:p.Pro1583Ser
NM_001184985.1:c.4771C>T	NP_001171914.1:p.Pro1591Ser
NM_001184985.2:c.4771C>T	NP_001171914.1:p.Pro1591Ser
NM_014823.2:c.3250C>T	NP_055638.2:p.Pro1084Ser
NM_014823.3:c.3250C>T	NP_055638.2:p.Pro1084Ser
NM_018979.3:c.3991C>T	NP_061852.3:p.Pro1331Ser
NM_213655.4:c.4747C>T	NP_998820.3:p.Pro1583Ser
ENST00000315939.10:c.3991C>T	ENSP00000313059.6:p.Pro1331Ser
ENST00000340908.8:c.4747C>T	ENSP00000341292.5:p.Pro1583Ser
ENST00000530271.6:c.5230C>T	ENSP00000433548.3:p.Pro1744Ser
ENST00000535572.5:c.3250C>T	ENSP00000441972.1:p.Pro1084Ser
ENST00000537687.5:c.4771C>T	ENSP00000444465.1:p.Pro1591Ser
ENST00000674810.1:n.4588C>T
ENST00000675236.1:n.2886C>T
ENST00000675631.1:c.2770C>T	ENSP00000502415.1:p.Pro924Ser
ENST00000676347.1:c.1438C>T	ENSP00000501875.1:p.Pro480Ser
XM_006719003.1:c.3988C>T	XP_006719066.1:p.Pro1330Ser
XM_006719003.2:c.3988C>T	XP_006719066.1:p.Pro1330Ser
XM_011520997.1:c.5230C>T	XP_011519299.1:p.Pro1744Ser
XM_011520997.3:c.5230C>T	XP_011519299.1:p.Pro1744Ser
XM_011520998.1:c.5227C>T	XP_011519300.1:p.Pro1743Ser
XM_011520998.2:c.5227C>T	XP_011519300.1:p.Pro1743Ser
XM_011520999.1:c.5230C>T	XP_011519301.1:p.Pro1744Ser
XM_011520999.2:c.5230C>T	XP_011519301.1:p.Pro1744Ser
XM_011521000.1:c.5230C>T	XP_011519302.1:p.Pro1744Ser
XM_011521000.2:c.5230C>T	XP_011519302.1:p.Pro1744Ser
XM_011521001.1:c.4951C>T	XP_011519303.1:p.Pro1651Ser
XM_011521001.2:c.4951C>T	XP_011519303.1:p.Pro1651Ser
XM_011521002.1:c.4768C>T	XP_011519304.1:p.Pro1590Ser
XM_011521002.2:c.4768C>T	XP_011519304.1:p.Pro1590Ser
XM_011521003.1:c.4492C>T	XP_011519305.1:p.Pro1498Ser
XM_011521003.2:c.4492C>T	XP_011519305.1:p.Pro1498Ser
XM_011521004.1:c.4489C>T	XP_011519306.1:p.Pro1497Ser
XM_011521004.2:c.4489C>T	XP_011519306.1:p.Pro1497Ser
XM_011521005.1:c.4009C>T	XP_011519307.1:p.Pro1337Ser
XM_011521005.2:c.4009C>T	XP_011519307.1:p.Pro1337Ser
XM_011521006.1:c.3907C>T	XP_011519308.1:p.Pro1303Ser
XM_011521006.2:c.3907C>T	XP_011519308.1:p.Pro1303Ser
XM_011521007.1:c.3904C>T	XP_011519309.1:p.Pro1302Ser
XM_011521007.2:c.3904C>T	XP_011519309.1:p.Pro1302Ser
XM_011521008.1:c.3169C>T	XP_011519310.1:p.Pro1057Ser
XM_011521008.2:c.3169C>T	XP_011519310.1:p.Pro1057Ser
XM_011521009.1:c.3166C>T	XP_011519311.1:p.Pro1056Ser
XM_011521009.2:c.3166C>T	XP_011519311.1:p.Pro1056Ser
XM_017019834.1:c.3529C>T	XP_016875323.1:p.Pro1177Ser
XM_017019835.1:c.3448C>T	XP_016875324.1:p.Pro1150Ser
XM_017019836.1:c.3445C>T	XP_016875325.1:p.Pro1149Ser
XM_017019837.1:c.3253C>T	XP_016875326.1:p.Pro1085Ser
XM_017019838.1:c.3250C>T	XP_016875327.1:p.Pro1084Ser
XM_017019839.1:c.3169C>T	XP_016875328.1:p.Pro1057Ser