Canonical Allele Identifier: CA346719375
Gene: CALM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47162309C>T , CM000664.2:g.47162309C>T GRCh38
NC_000002.11:g.47389448C>T , CM000664.1:g.47389448C>T GRCh37
NC_000002.10:g.47242952C>T NCBI36
NG_042065.1:g.19628G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272298.12:c.262G>A MANE Select ENSP00000272298.7:p.Glu88Lys
ENST00000456319.6:c.154G>A ENSP00000411440.2:p.Glu52Lys
ENST00000652974.1:c.*246G>A ENSP00000499369.1:n.*246G>A
ENST00000655450.1:c.154G>A ENSP00000499266.1:p.Glu52Lys
ENST00000655728.1:c.154G>A ENSP00000499656.1:p.Glu52Lys
ENST00000656538.1:c.154G>A ENSP00000499357.1:p.Glu52Lys
ENST00000668667.1:c.154G>A ENSP00000499706.1:p.Glu52Lys
ENST00000670593.1:n.1167G>A
ENST00000272298.11:c.262G>A ENSP00000272298.7:p.Glu88Lys
ENST00000409563.5:c.403G>A ENSP00000387065.1:p.Glu135Lys
ENST00000422269.1:c.102+8425G>A
ENST00000432899.5:c.178+210G>A ENSP00000406112.1:n.178+210G>A
ENST00000456319.5:c.376G>A ENSP00000411440.1:p.Glu126Lys
ENST00000460218.5:n.3702G>A
ENST00000482532.5:n.1529G>A
ENST00000484408.5:n.523G>A
ENST00000489742.1:n.499G>A
ENST00000628793.2:c.165+223G>A ENSP00000486952.1:n.165+223G>A
NM_001305624.1:c.406G>A NP_001292553.1:p.Glu136Lys
NM_001305625.1:c.154G>A NP_001292554.1:p.Glu52Lys
NM_001305626.1:c.154G>A NP_001292555.1:p.Glu52Lys
NM_001743.4:c.262G>A NP_001734.1:p.Glu88Lys
NM_001743.5:c.262G>A NP_001734.1:p.Glu88Lys
NM_001743.6:c.262G>A MANE Select NP_001734.1:p.Glu88Lys
NM_001305625.2:c.154G>A NP_001292554.1:p.Glu52Lys