Canonical Allele Identifier: CA8584227

Gene: WNK4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42788803G>C , CM000679.2:g.42788803G>C	GRCh38
NC_000017.10:g.40940821G>C , CM000679.1:g.40940821G>C	GRCh37
NC_000017.9:g.38194347G>C	NCBI36
NG_016227.1:g.13173G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032387.5:c.2157+6G>C MANE Select	NP_115763.2:n.2157+6G>C
ENST00000246914.10:c.2157+6G>C MANE Select	ENSP00000246914.4:n.2157+6G>C
NM_001321299.1:c.1149+6G>C	NP_001308228.1:n.1149+6G>C
NM_001321299.2:c.1149+6G>C	NP_001308228.1:n.1149+6G>C
NM_032387.4:c.2157+6G>C	NP_115763.2:n.2157+6G>C
ENST00000246914.9:c.2157+6G>C	ENSP00000246914.4:n.2157+6G>C
ENST00000591448.5:c.*658+6G>C	ENSP00000467088.1:n.*658+6G>C
ENST00000592072.1:n.715+6G>C
XM_005257595.3:c.2157+6G>C	XP_005257652.1:n.2157+6G>C
XM_005257596.2:c.2157+6G>C	XP_005257653.1:n.2157+6G>C
XM_005257597.3:c.2157+6G>C	XP_005257654.1:n.2157+6G>C
XM_006722020.2:c.2157+6G>C	XP_006722083.1:n.2157+6G>C
XM_006722021.1:c.1149+6G>C	XP_006722084.1:n.1149+6G>C
XM_006722022.1:c.1149+6G>C	XP_006722085.1:n.1149+6G>C
XM_011525132.1:c.2157+6G>C	XP_011523434.1:n.2157+6G>C
XM_011525133.1:c.2157+6G>C	XP_011523435.1:n.2157+6G>C
XM_011525134.1:c.2157+6G>C	XP_011523436.1:n.2157+6G>C
XM_011525135.1:c.2157+6G>C	XP_011523437.1:n.2157+6G>C
XM_017024962.1:c.2157+6G>C	XP_016880451.1:n.2157+6G>C
XM_017024966.1:c.1149+6G>C	XP_016880455.1:n.1149+6G>C