Canonical Allele Identifier: CA1219495598
Gene: CAMSAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.200857572T= , CM000663.2:g.200857572T= GRCh38
NC_000001.10:g.200826700T= , CM000663.1:g.200826700T= GRCh37
NC_000001.9:g.199093323T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000358823.7:c.4131+148T= MANE Select ENSP00000351684.2:n.4131+148T=
ENST00000236925.8:c.4164+148T= ENSP00000236925.4:n.4164+148T=
ENST00000358823.6:c.4131+148T= ENSP00000351684.2:n.4131+148T=
ENST00000413307.6:c.4083+148T= ENSP00000416800.2:n.4083+148T=
ENST00000475326.1:c.299T=
NM_001297707.1:c.4164+148T= NP_001284636.1:n.4164+148T=
NM_001297708.1:c.4083+148T= NP_001284637.1:n.4083+148T=
NM_203459.2:c.4131+148T= NP_982284.1:n.4131+148T=
XM_005245041.2:c.4116+148T= XP_005245098.1:n.4116+148T=
XM_005245041.3:c.4116+148T= XP_005245098.1:n.4116+148T=
XM_017000799.1:c.3831+148T= XP_016856288.1:n.3831+148T=
NM_001297707.2:c.4164+148T= NP_001284636.1:n.4164+148T=
NM_001297708.2:c.4083+148T= NP_001284637.1:n.4083+148T=
NM_203459.3:c.4131+148T= NP_982284.1:n.4131+148T=
NM_001297707.3:c.4164+148T= NP_001284636.1:n.4164+148T=
NM_001297708.3:c.4083+148T= NP_001284637.1:n.4083+148T=
NM_001389638.1:c.4116+148T= NP_001376567.1:n.4116+148T=
NM_203459.4:c.4131+148T= MANE Select NP_982284.1:n.4131+148T=