Canonical Allele Identifier: CA413339311

Gene: WNK3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54232955C>T , CM000685.2:g.54232955C>T	GRCh38
NC_000023.10:g.54259388C>T , CM000685.1:g.54259388C>T	GRCh37
NC_000023.9:g.54276113C>T	NCBI36
NG_021259.1:g.130051G>A
NG_021259.2:g.130051G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020922.5:c.4694G>A MANE Select	NP_065973.2:p.Arg1565His
ENST00000354646.7:c.4694G>A MANE Select	ENSP00000346667.2:p.Arg1565His
NM_001002838.3:c.4553G>A	NP_001002838.1:p.Arg1518His
NM_001002838.4:c.4553G>A	NP_001002838.1:p.Arg1518His
NM_001395166.1:c.4553G>A	NP_001382095.1:p.Arg1518His
NM_020922.4:c.4694G>A	NP_065973.2:p.Arg1565His
ENST00000354646.6:c.4694G>A	ENSP00000346667.2:p.Arg1565His
ENST00000375159.6:c.4694G>A	ENSP00000364301.2:p.Arg1565His
ENST00000375169.7:c.4553G>A	ENSP00000364312.3:p.Arg1518His
ENST00000620763.1:c.4694G>A	ENSP00000481888.1:p.Arg1565His
XM_006724593.2:c.4553G>A	XP_006724656.1:p.Arg1518His
XM_006724593.3:c.4553G>A	XP_006724656.1:p.Arg1518His
XM_011530802.1:c.4553G>A	XP_011529104.1:p.Arg1518His
XM_011530802.2:c.4553G>A	XP_011529104.1:p.Arg1518His
XM_011530803.1:c.4553G>A	XP_011529105.1:p.Arg1518His
XM_011530804.1:c.4553G>A	XP_011529106.1:p.Arg1518His
XM_011530805.1:c.4553G>A	XP_011529107.1:p.Arg1518His
XM_011530806.1:c.4553G>A	XP_011529108.1:p.Arg1518His
XM_011530807.1:c.2519G>A	XP_011529109.1:p.Arg840His
XM_017029741.1:c.4694G>A	XP_016885230.1:p.Arg1565His
XM_017029742.1:c.4694G>A	XP_016885231.1:p.Arg1565His
XM_017029743.1:c.4694G>A	XP_016885232.1:p.Arg1565His
XM_017029744.1:c.4694G>A	XP_016885233.1:p.Arg1565His
XM_017029745.1:c.4694G>A	XP_016885234.1:p.Arg1565His