Canonical Allele Identifier: CA1980477924

Gene: CHKA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68066076C= , CM000673.2:g.68066076C=	GRCh38
NC_000011.9:g.67833543C= , CM000673.1:g.67833543C=	GRCh37
NC_000011.8:g.67590119C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265689.9:c.1017-182G= MANE Select	ENSP00000265689.4:n.1017-182G=
ENST00000265689.8:c.1017-182G=	ENSP00000265689.4:n.1017-182G=
ENST00000356135.9:c.963-182G=	ENSP00000348454.4:n.963-182G=
ENST00000525155.5:c.33-182G=	ENSP00000432631.1:n.33-182G=
NM_001277.2:c.1017-182G=	NP_001268.2:n.1017-182G=
NM_212469.1:c.963-182G=	NP_997634.1:n.963-182G=
XR_428904.2:n.1228-182G=
XR_428905.1:n.2587-182G=
XR_949772.1:n.1174-182G=
XR_949773.1:n.1114-182G=
XR_949774.1:n.1945-182G=
XR_949775.1:n.2473-182G=
XR_949776.1:n.403-182G=
XR_949777.1:n.1326-182G=
XM_017017147.1:c.903-182G=	XP_016872636.1:n.903-182G=
XM_017017148.2:c.489-182G=	XP_016872637.1:n.489-182G=
XR_428904.3:n.1229-182G=
XR_428905.3:n.6801-182G=
XR_949772.2:n.1157-182G=
XR_949773.2:n.1115-182G=
NM_001277.3:c.1017-182G= MANE Select	NP_001268.2:n.1017-182G=
NM_001376219.1:c.1047-182G=	NP_001363148.1:n.1047-182G=
NM_001376220.1:c.903-182G=	NP_001363149.1:n.903-182G=
NM_001376221.1:c.651-182G=	NP_001363150.1:n.651-182G=
NM_001376222.1:c.597-182G=	NP_001363151.1:n.597-182G=
NM_212469.2:c.963-182G=	NP_997634.1:n.963-182G=
NR_164782.1:n.1228-182G=