Canonical Allele Identifier: CA346719352

Gene: CALM2

Linked Data

• MyVariant Identifiers: chr2:g.47389439G>T (hg19) ; chr2:g.47162300G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47162300G>T , CM000664.2:g.47162300G>T	GRCh38
NC_000002.11:g.47389439G>T , CM000664.1:g.47389439G>T	GRCh37
NC_000002.10:g.47242943G>T	NCBI36
NG_042065.1:g.19637C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000272298.12:c.271C>A MANE Select	ENSP00000272298.7:p.Arg91Ser
ENST00000456319.6:c.163C>A	ENSP00000411440.2:p.Arg55Ser
ENST00000652974.1:c.*255C>A	ENSP00000499369.1:n.*255C>A
ENST00000655450.1:c.163C>A	ENSP00000499266.1:p.Arg55Ser
ENST00000655728.1:c.163C>A	ENSP00000499656.1:p.Arg55Ser
ENST00000656538.1:c.163C>A	ENSP00000499357.1:p.Arg55Ser
ENST00000668667.1:c.163C>A	ENSP00000499706.1:p.Arg55Ser
ENST00000670593.1:n.1176C>A
ENST00000272298.11:c.271C>A	ENSP00000272298.7:p.Arg91Ser
ENST00000409563.5:c.412C>A	ENSP00000387065.1:p.Arg138Ser
ENST00000422269.1:c.102+8434C>A
ENST00000432899.5:c.178+219C>A	ENSP00000406112.1:n.178+219C>A
ENST00000456319.5:c.385C>A	ENSP00000411440.1:p.Arg129Ser
ENST00000460218.5:n.3711C>A
ENST00000482532.5:n.1538C>A
ENST00000484408.5:n.532C>A
ENST00000489742.1:n.508C>A
ENST00000628793.2:c.165+232C>A	ENSP00000486952.1:n.165+232C>A
NM_001305624.1:c.415C>A	NP_001292553.1:p.Arg139Ser
NM_001305625.1:c.163C>A	NP_001292554.1:p.Arg55Ser
NM_001305626.1:c.163C>A	NP_001292555.1:p.Arg55Ser
NM_001743.4:c.271C>A	NP_001734.1:p.Arg91Ser
NM_001743.5:c.271C>A	NP_001734.1:p.Arg91Ser
NM_001743.6:c.271C>A MANE Select	NP_001734.1:p.Arg91Ser
NM_001305625.2:c.163C>A	NP_001292554.1:p.Arg55Ser