Canonical Allele Identifier: CA1648573
Gene: CALM2 HGNC NCBI

Linked Data

dbSNP Id: rs777622236

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47162400_47162401del , CM000664.2:g.47162400_47162401del GRCh38
NC_000002.11:g.47389539_47389540del , CM000664.1:g.47389539_47389540del GRCh37
NC_000002.10:g.47243043_47243044del NCBI36
NG_042065.1:g.19536_19537del

Transcript Alleles

HGVS Amino-acid change
ENST00000272298.12:c.179-9_179-8del MANE Select ENSP00000272298.7:n.179-9_179-8del
ENST00000456319.6:c.71-9_71-8del ENSP00000411440.2:n.71-9_71-8del
ENST00000652974.1:c.*163-9_*163-8del ENSP00000499369.1:n.*163-9_*163-8del
ENST00000655450.1:c.71-9_71-8del ENSP00000499266.1:n.71-9_71-8del
ENST00000655728.1:c.71-9_71-8del ENSP00000499656.1:n.71-9_71-8del
ENST00000656538.1:c.71-9_71-8del ENSP00000499357.1:n.71-9_71-8del
ENST00000668667.1:c.71-9_71-8del ENSP00000499706.1:n.71-9_71-8del
ENST00000670593.1:n.1084-9_1084-8del
ENST00000272298.11:c.179-9_179-8del ENSP00000272298.7:n.179-9_179-8del
ENST00000409563.5:c.320-9_320-8del ENSP00000387065.1:n.320-9_320-8del
ENST00000422269.1:c.102+8333_102+8334del
ENST00000432899.5:c.178+118_178+119del ENSP00000406112.1:n.178+118_178+119del
ENST00000456319.5:c.293-9_293-8del ENSP00000411440.1:n.293-9_293-8del
ENST00000460218.5:n.3619-9_3619-8del
ENST00000482532.5:n.1446-9_1446-8del
ENST00000484408.5:n.440-9_440-8del
ENST00000489742.1:n.416-9_416-8del
ENST00000628793.2:c.165+131_165+132del ENSP00000486952.1:n.165+131_165+132del
NM_001305624.1:c.323-9_323-8del NP_001292553.1:n.323-9_323-8del
NM_001305625.1:c.71-9_71-8del NP_001292554.1:n.71-9_71-8del
NM_001305626.1:c.71-9_71-8del NP_001292555.1:n.71-9_71-8del
NM_001743.4:c.179-9_179-8del NP_001734.1:n.179-9_179-8del
NM_001743.5:c.179-9_179-8del NP_001734.1:n.179-9_179-8del
NM_001743.6:c.179-9_179-8del MANE Select NP_001734.1:n.179-9_179-8del
NM_001305625.2:c.71-9_71-8del NP_001292554.1:n.71-9_71-8del