Canonical Allele Identifier: CA2649730434

Gene: CAMSAP2

Linked Data

• gnomAD v4: 1-200857640-AAAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200857644_200857646del , CM000663.2:g.200857644_200857646del	GRCh38
NC_000001.10:g.200826772_200826774del , CM000663.1:g.200826772_200826774del	GRCh37
NC_000001.9:g.199093395_199093397del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358823.7:c.4132-110_4132-108del MANE Select	ENSP00000351684.2:n.4132-110_4132-108del
ENST00000236925.8:c.4165-110_4165-108del	ENSP00000236925.4:n.4165-110_4165-108del
ENST00000358823.6:c.4132-110_4132-108del	ENSP00000351684.2:n.4132-110_4132-108del
ENST00000413307.6:c.4084-110_4084-108del	ENSP00000416800.2:n.4084-110_4084-108del
ENST00000475326.1:c.371_373del
NM_001297707.1:c.4165-110_4165-108del	NP_001284636.1:n.4165-110_4165-108del
NM_001297708.1:c.4084-110_4084-108del	NP_001284637.1:n.4084-110_4084-108del
NM_203459.2:c.4132-110_4132-108del	NP_982284.1:n.4132-110_4132-108del
XM_005245041.2:c.4117-110_4117-108del	XP_005245098.1:n.4117-110_4117-108del
XM_005245041.3:c.4117-110_4117-108del	XP_005245098.1:n.4117-110_4117-108del
XM_017000799.1:c.3832-110_3832-108del	XP_016856288.1:n.3832-110_3832-108del
NM_001297707.2:c.4165-110_4165-108del	NP_001284636.1:n.4165-110_4165-108del
NM_001297708.2:c.4084-110_4084-108del	NP_001284637.1:n.4084-110_4084-108del
NM_203459.3:c.4132-110_4132-108del	NP_982284.1:n.4132-110_4132-108del
NM_001297707.3:c.4165-110_4165-108del	NP_001284636.1:n.4165-110_4165-108del
NM_001297708.3:c.4084-110_4084-108del	NP_001284637.1:n.4084-110_4084-108del
NM_001389638.1:c.4117-110_4117-108del	NP_001376567.1:n.4117-110_4117-108del
NM_203459.4:c.4132-110_4132-108del MANE Select	NP_982284.1:n.4132-110_4132-108del