Canonical Allele Identifier: CA7305786

Gene: CALM1

Linked Data

• dbSNP Id: rs768639240
• ExAC: 14:90870684 A / G
• gnomAD v2: 14-90870684-A-G
• gnomAD v3: 14-90404340-A-G
• gnomAD v4: 14-90404340-A-G
• MyVariant Identifiers: chr14:g.90870684A>G (hg19) ; chr14:g.90404340A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404340A>G , CM000676.2:g.90404340A>G	GRCh38
NC_000014.8:g.90870684A>G , CM000676.1:g.90870684A>G	GRCh37
NC_000014.7:g.89940437A>G	NCBI36
NG_013338.1:g.12358A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.286-39A>G MANE Select	ENSP00000349467.4:n.286-39A>G
ENST00000447653.8:c.178-39A>G	ENSP00000403491.4:n.178-39A>G
ENST00000659177.1:c.178-39A>G	ENSP00000499421.1:n.178-39A>G
ENST00000663135.1:c.178-39A>G	ENSP00000499498.1:n.178-39A>G
ENST00000356978.8:c.286-39A>G	ENSP00000349467.4:n.286-39A>G
ENST00000447653.7:c.289-39A>G	ENSP00000403491.3:n.289-39A>G
ENST00000544280.6:c.178-39A>G	ENSP00000442853.2:n.178-39A>G
ENST00000553422.1:c.178-59A>G	ENSP00000450425.1:n.178-59A>G
ENST00000553542.5:c.178-39A>G	ENSP00000450829.1:n.178-39A>G
ENST00000553630.1:c.179-39A>G	ENSP00000451646.1:n.179-39A>G
ENST00000553964.5:n.2416-39A>G
ENST00000554296.1:n.338-39A>G
ENST00000556721.1:n.173A>G
ENST00000557020.5:c.178-39A>G	ENSP00000451062.1:n.178-39A>G
ENST00000626705.2:c.166-117A>G	ENSP00000486402.1:n.166-117A>G
NM_006888.4:c.286-39A>G	NP_008819.1:n.286-39A>G
XM_006720258.2:c.289-39A>G	XP_006720321.1:n.289-39A>G
NM_001363669.1:c.178-39A>G	NP_001350598.1:n.178-39A>G
NM_001363670.1:c.289-39A>G	NP_001350599.1:n.289-39A>G
NM_006888.5:c.286-39A>G	NP_008819.1:n.286-39A>G
NM_006888.6:c.286-39A>G MANE Select	NP_008819.1:n.286-39A>G
NM_001363669.2:c.178-39A>G	NP_001350598.1:n.178-39A>G
NM_001363670.2:c.289-39A>G	NP_001350599.1:n.289-39A>G