Canonical Allele Identifier: CA346719384

Gene: CALM2

Linked Data

• MyVariant Identifiers: chr2:g.47389452A>C (hg19) ; chr2:g.47162313A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47162313A>C , CM000664.2:g.47162313A>C	GRCh38
NC_000002.11:g.47389452A>C , CM000664.1:g.47389452A>C	GRCh37
NC_000002.10:g.47242956A>C	NCBI36
NG_042065.1:g.19624T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272298.12:c.258T>G MANE Select	ENSP00000272298.7:p.Ile86Met
ENST00000456319.6:c.150T>G	ENSP00000411440.2:p.Ile50Met
ENST00000652974.1:c.*242T>G	ENSP00000499369.1:n.*242T>G
ENST00000655450.1:c.150T>G	ENSP00000499266.1:p.Ile50Met
ENST00000655728.1:c.150T>G	ENSP00000499656.1:p.Ile50Met
ENST00000656538.1:c.150T>G	ENSP00000499357.1:p.Ile50Met
ENST00000668667.1:c.150T>G	ENSP00000499706.1:p.Ile50Met
ENST00000670593.1:n.1163T>G
ENST00000272298.11:c.258T>G	ENSP00000272298.7:p.Ile86Met
ENST00000409563.5:c.399T>G	ENSP00000387065.1:p.Ile133Met
ENST00000422269.1:c.102+8421T>G
ENST00000432899.5:c.178+206T>G	ENSP00000406112.1:n.178+206T>G
ENST00000456319.5:c.372T>G	ENSP00000411440.1:p.Ile124Met
ENST00000460218.5:n.3698T>G
ENST00000482532.5:n.1525T>G
ENST00000484408.5:n.519T>G
ENST00000489742.1:n.495T>G
ENST00000628793.2:c.165+219T>G	ENSP00000486952.1:n.165+219T>G
NM_001305624.1:c.402T>G	NP_001292553.1:p.Ile134Met
NM_001305625.1:c.150T>G	NP_001292554.1:p.Ile50Met
NM_001305626.1:c.150T>G	NP_001292555.1:p.Ile50Met
NM_001743.4:c.258T>G	NP_001734.1:p.Ile86Met
NM_001743.5:c.258T>G	NP_001734.1:p.Ile86Met
NM_001743.6:c.258T>G MANE Select	NP_001734.1:p.Ile86Met
NM_001305625.2:c.150T>G	NP_001292554.1:p.Ile50Met