Canonical Allele Identifier: CA1142523467

Gene: CAPZB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19438987A= , CM000663.2:g.19438987A=	GRCh38
NC_000001.10:g.19765481A= , CM000663.1:g.19765481A=	GRCh37
NC_000001.9:g.19638068A=	NCBI36
NG_029551.1:g.51586T=
NG_029551.2:g.51586T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375142.6:c.4-19237T=	ENSP00000364284.1:n.4-19237T=
ENST00000264202.8:c.4-19237T= MANE Select	ENSP00000264202.7:n.4-19237T=
ENST00000375144.6:c.4-19237T=	ENSP00000364286.2:n.4-19237T=
ENST00000482808.2:n.103-19237T=
ENST00000674390.1:n.703-19237T=
ENST00000674432.1:c.4-19237T=	ENSP00000501528.1:n.4-19237T=
ENST00000674449.1:c.4-19237T=	ENSP00000501388.1:n.4-19237T=
ENST00000264202.7:c.4-19237T=	ENSP00000264202.7:n.4-19237T=
ENST00000264203.7:c.81+9847T=	ENSP00000264203.3:n.81+9847T=
ENST00000375142.5:c.4-19237T=	ENSP00000364284.1:n.4-19237T=
ENST00000433834.5:c.91-19237T=	ENSP00000401010.1:n.91-19237T=
ENST00000459967.6:n.104+46449T=
ENST00000482808.1:n.54-19237T=
NM_001206540.2:c.4-19237T=	NP_001193469.1:n.4-19237T=
NM_001206541.2:c.81+9847T=	NP_001193470.1:n.81+9847T=
NM_001282162.1:c.91-19237T=	NP_001269091.1:n.91-19237T=
NM_001313932.1:c.4-19237T=	NP_001300861.1:n.4-19237T=
NM_004930.4:c.4-19237T=	NP_004921.1:n.4-19237T=
XM_006710938.2:c.84+13146T=	XP_006711001.1:n.84+13146T=
XM_011542228.1:c.91-19237T=	XP_011540530.1:n.91-19237T=
XR_947021.1:n.912A=
XM_006710938.4:c.84+13146T=	XP_006711001.1:n.84+13146T=
XM_011542228.3:c.91-19237T=	XP_011540530.1:n.91-19237T=
XM_017002428.2:c.-33-19237T=	XP_016857917.1:n.-33-19237T=
XM_017002429.2:c.91-19237T=	XP_016857918.1:n.91-19237T=
XM_017002430.2:c.91-19237T=	XP_016857919.1:n.91-19237T=
NM_004930.5:c.4-19237T= MANE Select	NP_004921.1:n.4-19237T=
NM_001206540.3:c.4-19237T=	NP_001193469.1:n.4-19237T=
NM_001206541.3:c.81+9847T=	NP_001193470.1:n.81+9847T=
NM_001282162.2:c.91-19237T=	NP_001269091.1:n.91-19237T=
NM_001313932.2:c.4-19237T=	NP_001300861.1:n.4-19237T=