Canonical Allele Identifier: CA2495693704
Gene: CALM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47162407T= , CM000664.2:g.47162407T= GRCh38
NC_000002.11:g.47389546T= , CM000664.1:g.47389546T= GRCh37
NC_000002.10:g.47243050T= NCBI36
NG_042065.1:g.19530A=

Transcript Alleles

HGVS Amino-acid change
ENST00000272298.12:c.179-15A= MANE Select ENSP00000272298.7:n.179-15A=
ENST00000456319.6:c.71-15A= ENSP00000411440.2:n.71-15A=
ENST00000652974.1:c.*163-15A= ENSP00000499369.1:n.*163-15A=
ENST00000655450.1:c.71-15A= ENSP00000499266.1:n.71-15A=
ENST00000655728.1:c.71-15A= ENSP00000499656.1:n.71-15A=
ENST00000656538.1:c.71-15A= ENSP00000499357.1:n.71-15A=
ENST00000668667.1:c.71-15A= ENSP00000499706.1:n.71-15A=
ENST00000670593.1:n.1084-15A=
ENST00000272298.11:c.179-15A= ENSP00000272298.7:n.179-15A=
ENST00000409563.5:c.320-15A= ENSP00000387065.1:n.320-15A=
ENST00000422269.1:c.102+8327A=
ENST00000432899.5:c.178+112A= ENSP00000406112.1:n.178+112A=
ENST00000456319.5:c.293-15A= ENSP00000411440.1:n.293-15A=
ENST00000460218.5:n.3619-15A=
ENST00000482532.5:n.1446-15A=
ENST00000484408.5:n.440-15A=
ENST00000489742.1:n.416-15A=
ENST00000628793.2:c.165+125A= ENSP00000486952.1:n.165+125A=
NM_001305624.1:c.323-15A= NP_001292553.1:n.323-15A=
NM_001305625.1:c.71-15A= NP_001292554.1:n.71-15A=
NM_001305626.1:c.71-15A= NP_001292555.1:n.71-15A=
NM_001743.4:c.179-15A= NP_001734.1:n.179-15A=
NM_001743.5:c.179-15A= NP_001734.1:n.179-15A=
NM_001743.6:c.179-15A= MANE Select NP_001734.1:n.179-15A=
NM_001305625.2:c.71-15A= NP_001292554.1:n.71-15A=