Canonical Allele Identifier: CA2495693336

Gene: CALM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47161744C= , CM000664.2:g.47161744C=	GRCh38
NC_000002.11:g.47388883C= , CM000664.1:g.47388883C=	GRCh37
NC_000002.10:g.47242387C=	NCBI36
NG_042065.1:g.20193G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272298.12:c.400G= MANE Select	ENSP00000272298.7:p.Asp134=
ENST00000456319.6:c.292G=	ENSP00000411440.2:p.Asp98=
ENST00000652974.1:c.*384G=	ENSP00000499369.1:n.*384G=
ENST00000655450.1:c.292G=	ENSP00000499266.1:p.Asp98=
ENST00000655728.1:c.292G=	ENSP00000499656.1:p.Asp98=
ENST00000656538.1:c.292G=	ENSP00000499357.1:p.Asp98=
ENST00000668667.1:c.292G=	ENSP00000499706.1:p.Asp98=
ENST00000670593.1:n.1305G=
ENST00000272298.11:c.400G=	ENSP00000272298.7:p.Asp134=
ENST00000409563.5:c.541G=	ENSP00000387065.1:p.Asp181=
ENST00000422269.1:c.103-8728G=
ENST00000432899.5:c.*95G=	ENSP00000406112.1:n.*95G=
ENST00000456319.5:c.514G=	ENSP00000411440.1:p.Asp172=
ENST00000460218.5:n.3840G=
ENST00000482532.5:n.1667G=
ENST00000484408.5:n.661G=
ENST00000628793.2:c.202G=	ENSP00000486952.1:p.Asp68=
NM_001305624.1:c.544G=	NP_001292553.1:p.Asp182=
NM_001305625.1:c.292G=	NP_001292554.1:p.Asp98=
NM_001305626.1:c.292G=	NP_001292555.1:p.Asp98=
NM_001743.4:c.400G=	NP_001734.1:p.Asp134=
NM_001743.5:c.400G=	NP_001734.1:p.Asp134=
NM_001743.6:c.400G= MANE Select	NP_001734.1:p.Asp134=
NM_001305625.2:c.292G=	NP_001292554.1:p.Asp98=