Canonical Allele Identifier: CA2495693333

Gene: CALM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47161737T= , CM000664.2:g.47161737T=	GRCh38
NC_000002.11:g.47388876T= , CM000664.1:g.47388876T=	GRCh37
NC_000002.10:g.47242380T=	NCBI36
NG_042065.1:g.20200A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272298.12:c.407A= MANE Select	ENSP00000272298.7:p.Gln136=
ENST00000456319.6:c.299A=	ENSP00000411440.2:p.Gln100=
ENST00000652974.1:c.*391A=	ENSP00000499369.1:n.*391A=
ENST00000655450.1:c.299A=	ENSP00000499266.1:p.Gln100=
ENST00000655728.1:c.299A=	ENSP00000499656.1:p.Gln100=
ENST00000656538.1:c.299A=	ENSP00000499357.1:p.Gln100=
ENST00000668667.1:c.299A=	ENSP00000499706.1:p.Gln100=
ENST00000670593.1:n.1312A=
ENST00000272298.11:c.407A=	ENSP00000272298.7:p.Gln136=
ENST00000409563.5:c.548A=	ENSP00000387065.1:p.Gln183=
ENST00000422269.1:c.103-8721A=
ENST00000432899.5:c.*102A=	ENSP00000406112.1:n.*102A=
ENST00000456319.5:c.521A=	ENSP00000411440.1:p.Gln174=
ENST00000460218.5:n.3847A=
ENST00000482532.5:n.1674A=
ENST00000484408.5:n.668A=
ENST00000628793.2:c.209A=	ENSP00000486952.1:p.Gln70=
NM_001305624.1:c.551A=	NP_001292553.1:p.Gln184=
NM_001305625.1:c.299A=	NP_001292554.1:p.Gln100=
NM_001305626.1:c.299A=	NP_001292555.1:p.Gln100=
NM_001743.4:c.407A=	NP_001734.1:p.Gln136=
NM_001743.5:c.407A=	NP_001734.1:p.Gln136=
NM_001743.6:c.407A= MANE Select	NP_001734.1:p.Gln136=
NM_001305625.2:c.299A=	NP_001292554.1:p.Gln100=