Canonical Allele Identifier: CA346719386

Gene: CALM2

Linked Data

• MyVariant Identifiers: chr2:g.47389453A>T (hg19) ; chr2:g.47162314A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47162314A>T , CM000664.2:g.47162314A>T	GRCh38
NC_000002.11:g.47389453A>T , CM000664.1:g.47389453A>T	GRCh37
NC_000002.10:g.47242957A>T	NCBI36
NG_042065.1:g.19623T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000272298.12:c.257T>A MANE Select	ENSP00000272298.7:p.Ile86Asn
ENST00000456319.6:c.149T>A	ENSP00000411440.2:p.Ile50Asn
ENST00000652974.1:c.*241T>A	ENSP00000499369.1:n.*241T>A
ENST00000655450.1:c.149T>A	ENSP00000499266.1:p.Ile50Asn
ENST00000655728.1:c.149T>A	ENSP00000499656.1:p.Ile50Asn
ENST00000656538.1:c.149T>A	ENSP00000499357.1:p.Ile50Asn
ENST00000668667.1:c.149T>A	ENSP00000499706.1:p.Ile50Asn
ENST00000670593.1:n.1162T>A
ENST00000272298.11:c.257T>A	ENSP00000272298.7:p.Ile86Asn
ENST00000409563.5:c.398T>A	ENSP00000387065.1:p.Ile133Asn
ENST00000422269.1:c.102+8420T>A
ENST00000432899.5:c.178+205T>A	ENSP00000406112.1:n.178+205T>A
ENST00000456319.5:c.371T>A	ENSP00000411440.1:p.Ile124Asn
ENST00000460218.5:n.3697T>A
ENST00000482532.5:n.1524T>A
ENST00000484408.5:n.518T>A
ENST00000489742.1:n.494T>A
ENST00000628793.2:c.165+218T>A	ENSP00000486952.1:n.165+218T>A
NM_001305624.1:c.401T>A	NP_001292553.1:p.Ile134Asn
NM_001305625.1:c.149T>A	NP_001292554.1:p.Ile50Asn
NM_001305626.1:c.149T>A	NP_001292555.1:p.Ile50Asn
NM_001743.4:c.257T>A	NP_001734.1:p.Ile86Asn
NM_001743.5:c.257T>A	NP_001734.1:p.Ile86Asn
NM_001743.6:c.257T>A MANE Select	NP_001734.1:p.Ile86Asn
NM_001305625.2:c.149T>A	NP_001292554.1:p.Ile50Asn