Canonical Allele Identifier: CA35994003

Gene: CAMSAP2

Linked Data

• dbSNP Id: rs895719037
• gnomAD v4: 1-200857541-A-T
• MyVariant Identifiers: chr1:g.200826669A>T (hg19) ; chr1:g.200857541A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200857541A>T , CM000663.2:g.200857541A>T	GRCh38
NC_000001.10:g.200826669A>T , CM000663.1:g.200826669A>T	GRCh37
NC_000001.9:g.199093292A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358823.7:c.4131+117A>T MANE Select	ENSP00000351684.2:n.4131+117A>T
ENST00000236925.8:c.4164+117A>T	ENSP00000236925.4:n.4164+117A>T
ENST00000358823.6:c.4131+117A>T	ENSP00000351684.2:n.4131+117A>T
ENST00000413307.6:c.4083+117A>T	ENSP00000416800.2:n.4083+117A>T
ENST00000475326.1:c.268A>T
NM_001297707.1:c.4164+117A>T	NP_001284636.1:n.4164+117A>T
NM_001297708.1:c.4083+117A>T	NP_001284637.1:n.4083+117A>T
NM_203459.2:c.4131+117A>T	NP_982284.1:n.4131+117A>T
XM_005245041.2:c.4116+117A>T	XP_005245098.1:n.4116+117A>T
XM_005245041.3:c.4116+117A>T	XP_005245098.1:n.4116+117A>T
XM_017000799.1:c.3831+117A>T	XP_016856288.1:n.3831+117A>T
NM_001297707.2:c.4164+117A>T	NP_001284636.1:n.4164+117A>T
NM_001297708.2:c.4083+117A>T	NP_001284637.1:n.4083+117A>T
NM_203459.3:c.4131+117A>T	NP_982284.1:n.4131+117A>T
NM_001297707.3:c.4164+117A>T	NP_001284636.1:n.4164+117A>T
NM_001297708.3:c.4083+117A>T	NP_001284637.1:n.4083+117A>T
NM_001389638.1:c.4116+117A>T	NP_001376567.1:n.4116+117A>T
NM_203459.4:c.4131+117A>T MANE Select	NP_982284.1:n.4131+117A>T