Canonical Allele Identifier: CA425961724

Gene: CALM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47170735T>C , CM000664.2:g.47170735T>C	GRCh38
NC_000002.11:g.47397874T>C , CM000664.1:g.47397874T>C	GRCh37
NC_000002.10:g.47251378T>C	NCBI36
NG_042065.1:g.11202A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001743.6:c.33A>G MANE Select	NP_001734.1:p.Ala11=
ENST00000272298.12:c.33A>G MANE Select	ENSP00000272298.7:p.Ala11=
NM_001305624.1:c.177A>G	NP_001292553.1:p.Ala59=
NM_001305625.1:c.-76A>G	NP_001292554.1:n.-76A>G
NM_001305625.2:c.-76A>G	NP_001292554.1:n.-76A>G
NM_001305626.1:c.-76A>G	NP_001292555.1:n.-76A>G
NM_001743.4:c.33A>G	NP_001734.1:p.Ala11=
NM_001743.5:c.33A>G	NP_001734.1:p.Ala11=
ENST00000272298.11:c.33A>G	ENSP00000272298.7:p.Ala11=
ENST00000409563.5:c.-42A>G	ENSP00000387065.1:n.-42A>G
ENST00000422269.1:c.101A>G
ENST00000432899.5:c.33A>G	ENSP00000406112.1:p.Ala11=
ENST00000456319.5:c.147A>G	ENSP00000411440.1:p.Ala49=
ENST00000456319.6:c.-76A>G	ENSP00000411440.2:n.-76A>G
ENST00000460218.5:n.3473A>G
ENST00000484408.5:n.294A>G
ENST00000489742.1:n.270A>G
ENST00000628793.2:c.33A>G	ENSP00000486952.1:p.Ala11=
ENST00000652974.1:c.*17A>G	ENSP00000499369.1:n.*17A>G
ENST00000655450.1:c.-76A>G	ENSP00000499266.1:n.-76A>G
ENST00000655728.1:c.-76A>G	ENSP00000499656.1:n.-76A>G
ENST00000656538.1:c.-76A>G	ENSP00000499357.1:n.-76A>G
ENST00000668667.1:c.-76A>G	ENSP00000499706.1:n.-76A>G