Canonical Allele Identifier: CA1157098183

Gene: CAPZB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19438939_19438940delinsAG , CM000663.2:g.19438939_19438940delinsAG	GRCh38
NC_000001.10:g.19765433_19765434delinsAG , CM000663.1:g.19765433_19765434delinsAG	GRCh37
NC_000001.9:g.19638020_19638021delinsAG	NCBI36
NG_029551.1:g.51633_51634delinsCT
NG_029551.2:g.51633_51634delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000375142.6:c.4-19190_4-19189delinsCT	ENSP00000364284.1:n.4-19190_4-19189delinsCT
ENST00000264202.8:c.4-19190_4-19189delinsCT MANE Select	ENSP00000264202.7:n.4-19190_4-19189delinsCT
ENST00000375144.6:c.4-19190_4-19189delinsCT	ENSP00000364286.2:n.4-19190_4-19189delinsCT
ENST00000482808.2:n.103-19190_103-19189delinsCT
ENST00000674390.1:n.703-19190_703-19189delinsCT
ENST00000674432.1:c.4-19190_4-19189delinsCT	ENSP00000501528.1:n.4-19190_4-19189delinsCT
ENST00000674449.1:c.4-19190_4-19189delinsCT	ENSP00000501388.1:n.4-19190_4-19189delinsCT
ENST00000264202.7:c.4-19190_4-19189delinsCT	ENSP00000264202.7:n.4-19190_4-19189delinsCT
ENST00000264203.7:c.81+9894_81+9895delinsCT	ENSP00000264203.3:n.81+9894_81+9895delinsCT
ENST00000375142.5:c.4-19190_4-19189delinsCT	ENSP00000364284.1:n.4-19190_4-19189delinsCT
ENST00000433834.5:c.91-19190_91-19189delinsCT	ENSP00000401010.1:n.91-19190_91-19189delinsCT
ENST00000459967.6:n.104+46496_104+46497delinsCT
ENST00000482808.1:n.54-19190_54-19189delinsCT
NM_001206540.2:c.4-19190_4-19189delinsCT	NP_001193469.1:n.4-19190_4-19189delinsCT
NM_001206541.2:c.81+9894_81+9895delinsCT	NP_001193470.1:n.81+9894_81+9895delinsCT
NM_001282162.1:c.91-19190_91-19189delinsCT	NP_001269091.1:n.91-19190_91-19189delinsCT
NM_001313932.1:c.4-19190_4-19189delinsCT	NP_001300861.1:n.4-19190_4-19189delinsCT
NM_004930.4:c.4-19190_4-19189delinsCT	NP_004921.1:n.4-19190_4-19189delinsCT
XM_006710938.2:c.84+13193_84+13194delinsCT	XP_006711001.1:n.84+13193_84+13194delinsCT
XM_011542228.1:c.91-19190_91-19189delinsCT	XP_011540530.1:n.91-19190_91-19189delinsCT
XR_947021.1:n.864_865delinsAG
XM_006710938.4:c.84+13193_84+13194delinsCT	XP_006711001.1:n.84+13193_84+13194delinsCT
XM_011542228.3:c.91-19190_91-19189delinsCT	XP_011540530.1:n.91-19190_91-19189delinsCT
XM_017002428.2:c.-33-19190_-33-19189delinsCT	XP_016857917.1:n.-33-19190_-33-19189delinsCT
XM_017002429.2:c.91-19190_91-19189delinsCT	XP_016857918.1:n.91-19190_91-19189delinsCT
XM_017002430.2:c.91-19190_91-19189delinsCT	XP_016857919.1:n.91-19190_91-19189delinsCT
NM_004930.5:c.4-19190_4-19189delinsCT MANE Select	NP_004921.1:n.4-19190_4-19189delinsCT
NM_001206540.3:c.4-19190_4-19189delinsCT	NP_001193469.1:n.4-19190_4-19189delinsCT
NM_001206541.3:c.81+9894_81+9895delinsCT	NP_001193470.1:n.81+9894_81+9895delinsCT
NM_001282162.2:c.91-19190_91-19189delinsCT	NP_001269091.1:n.91-19190_91-19189delinsCT
NM_001313932.2:c.4-19190_4-19189delinsCT	NP_001300861.1:n.4-19190_4-19189delinsCT