Canonical Allele Identifier: CA407752058

Gene: ZIK1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57590042A>G , CM000681.2:g.57590042A>G	GRCh38
NC_000019.9:g.58101410A>G , CM000681.1:g.58101410A>G	GRCh37
NC_000019.8:g.62793222A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001010879.4:c.231A>G MANE Select	NP_001010879.2:p.Thr77=
ENST00000597850.2:c.231A>G MANE Select	ENSP00000472867.1:p.Thr77=
NM_001010879.2:c.231A>G	NP_001010879.2:p.Thr77=
NM_001010879.3:c.231A>G	NP_001010879.2:p.Thr77=
NM_001321145.1:c.192A>G	NP_001308074.1:p.Thr64=
NM_001321145.2:c.192A>G	NP_001308074.1:p.Thr64=
NM_001321146.1:c.66A>G	NP_001308075.1:p.Thr22=
NM_001321146.2:c.66A>G	NP_001308075.1:p.Thr22=
NM_001321147.1:c.-79A>G	NP_001308076.1:n.-79A>G
NM_001321147.2:c.-79A>G	NP_001308076.1:n.-79A>G
ENST00000307468.4:c.65A>G	ENSP00000303820.4:p.His22Arg
ENST00000536878.6:c.192A>G	ENSP00000438487.1:p.Thr64=
ENST00000597850.1:c.231A>G	ENSP00000472867.1:p.Thr77=
ENST00000598689.1:c.150A>G	ENSP00000469971.1:p.Thr50=
ENST00000599456.1:c.66A>G	ENSP00000468937.1:p.Thr22=
ENST00000600053.5:c.174A>G	ENSP00000472088.1:p.Thr58=
XM_005258769.2:c.66A>G	XP_005258826.1:p.Thr22=
XM_011526760.1:c.192A>G	XP_011525062.1:p.Thr64=
XM_011526761.1:c.189A>G	XP_011525063.1:p.Thr63=
XM_011526762.1:c.174A>G	XP_011525064.1:p.Thr58=
XM_011526763.1:c.150A>G	XP_011525065.1:p.Thr50=
XM_011526764.1:c.132A>G	XP_011525066.1:p.Thr44=
XM_011526765.1:c.123A>G	XP_011525067.1:p.Thr41=
XM_011526765.2:c.123A>G	XP_011525067.1:p.Thr41=
XM_011526766.1:c.66A>G	XP_011525068.1:p.Thr22=
XM_011526766.2:c.66A>G	XP_011525068.1:p.Thr22=
XM_011526767.1:c.-79A>G	XP_011525069.1:n.-79A>G
XM_011526767.3:c.-79A>G	XP_011525069.1:n.-79A>G