Canonical Allele Identifier: CA10370983

Gene: ZFX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.24179647G>A , CM000685.2:g.24179647G>A	GRCh38
NC_000023.10:g.24197764G>A , CM000685.1:g.24197764G>A	GRCh37
NC_000023.9:g.24107685G>A	NCBI36
NG_021253.1:g.34911G>A
NG_021253.2:g.34911G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304543.10:c.523G>A MANE Select	ENSP00000304985.5:p.Val175Ile
ENST00000304543.9:c.523G>A	ENSP00000304985.5:p.Val175Ile
ENST00000338565.3:c.523G>A	ENSP00000343384.3:p.Val175Ile
ENST00000379177.5:c.523G>A	ENSP00000368475.1:p.Val175Ile
ENST00000379188.7:c.640G>A	ENSP00000368486.4:p.Val214Ile
ENST00000459724.1:n.278-27679G>A
ENST00000539115.5:c.-41-27679G>A	ENSP00000438233.1:n.-41-27679G>A
NM_001178084.1:c.523G>A	NP_001171555.1:p.Val175Ile
NM_001178085.1:c.523G>A	NP_001171556.1:p.Val175Ile
NM_001178086.1:c.-41-27679G>A	NP_001171557.1:n.-41-27679G>A
NM_001178095.1:c.523G>A	NP_001171566.1:p.Val175Ile
NM_003410.3:c.523G>A	NP_003401.2:p.Val175Ile
XM_005274591.3:c.523G>A	XP_005274648.1:p.Val175Ile
XM_005274592.2:c.523G>A	XP_005274649.1:p.Val175Ile
XM_005274594.3:c.448G>A	XP_005274651.1:p.Val150Ile
XM_006724513.2:c.640G>A	XP_006724576.1:p.Val214Ile
XM_006724515.2:c.640G>A	XP_006724578.1:p.Val214Ile
XM_011545577.1:c.640G>A	XP_011543879.1:p.Val214Ile
XM_011545578.1:c.640G>A	XP_011543880.1:p.Val214Ile
XM_011545579.1:c.523G>A	XP_011543881.1:p.Val175Ile
XM_011545580.1:c.523G>A	XP_011543882.1:p.Val175Ile
XM_011545581.1:c.523G>A	XP_011543883.1:p.Val175Ile
XM_011545582.1:c.448G>A	XP_011543884.1:p.Val150Ile
XM_011545583.1:c.448G>A	XP_011543885.1:p.Val150Ile
NM_001330327.1:c.640G>A	NP_001317256.1:p.Val214Ile
XM_005274591.4:c.523G>A	XP_005274648.1:p.Val175Ile
XM_005274592.3:c.523G>A	XP_005274649.1:p.Val175Ile
XM_005274594.5:c.448G>A	XP_005274651.1:p.Val150Ile
XM_006724513.3:c.640G>A	XP_006724576.1:p.Val214Ile
XM_011545581.2:c.523G>A	XP_011543883.1:p.Val175Ile
XM_011545583.3:c.556G>A	XP_011543885.2:p.Val186Ile
XM_017029788.1:c.640G>A	XP_016885277.1:p.Val214Ile
XM_017029789.1:c.640G>A	XP_016885278.1:p.Val214Ile
XM_017029790.1:c.640G>A	XP_016885279.1:p.Val214Ile
XM_017029791.2:c.640G>A	XP_016885280.1:p.Val214Ile
XM_017029792.1:c.640G>A	XP_016885281.1:p.Val214Ile
XM_017029793.1:c.640G>A	XP_016885282.1:p.Val214Ile
XM_017029794.1:c.523G>A	XP_016885283.1:p.Val175Ile
XM_017029795.1:c.523G>A	XP_016885284.1:p.Val175Ile
XM_017029796.1:c.640G>A	XP_016885285.1:p.Val214Ile
XM_017029797.2:c.448G>A	XP_016885286.1:p.Val150Ile
XM_017029798.2:c.448G>A	XP_016885287.1:p.Val150Ile
XM_017029799.1:c.523G>A	XP_016885288.1:p.Val175Ile
XM_017029800.2:c.448G>A	XP_016885289.1:p.Val150Ile
XM_024452440.1:c.640G>A	XP_024308208.1:p.Val214Ile
NM_001178084.2:c.523G>A	NP_001171555.1:p.Val175Ile
NM_001178095.2:c.523G>A	NP_001171566.1:p.Val175Ile
NM_001330327.2:c.640G>A	NP_001317256.1:p.Val214Ile
NM_003410.4:c.523G>A MANE Select	NP_003401.2:p.Val175Ile
NM_001178086.2:c.-41-27679G>A	NP_001171557.1:n.-41-27679G>A