Canonical Allele Identifier: CA2626079606

Gene: CALM1

Linked Data

• gnomAD v4: 14-90404610-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404610T>A , CM000676.2:g.90404610T>A	GRCh38
NC_000014.8:g.90870954T>A , CM000676.1:g.90870954T>A	GRCh37
NC_000014.7:g.89940707T>A	NCBI36
NG_013338.1:g.12628T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356978.9:c.422-79T>A MANE Select	ENSP00000349467.4:n.422-79T>A
ENST00000447653.8:c.314-79T>A	ENSP00000403491.4:n.314-79T>A
ENST00000659177.1:c.314-79T>A	ENSP00000499421.1:n.314-79T>A
ENST00000663135.1:c.314-79T>A	ENSP00000499498.1:n.314-79T>A
ENST00000356978.8:c.422-79T>A	ENSP00000349467.4:n.422-79T>A
ENST00000447653.7:c.425-79T>A	ENSP00000403491.3:n.425-79T>A
ENST00000544280.6:c.314-79T>A	ENSP00000442853.2:n.314-79T>A
ENST00000553422.1:c.294-79T>A	ENSP00000450425.1:n.294-79T>A
ENST00000553542.5:c.314-79T>A	ENSP00000450829.1:n.314-79T>A
ENST00000553630.1:c.*63-79T>A	ENSP00000451646.1:n.*63-79T>A
ENST00000553964.5:n.2552-79T>A
ENST00000554296.1:n.474-79T>A
ENST00000556721.1:n.348-79T>A
ENST00000626705.2:c.224-79T>A	ENSP00000486402.1:n.224-79T>A
NM_006888.4:c.422-79T>A	NP_008819.1:n.422-79T>A
XM_006720258.2:c.425-79T>A	XP_006720321.1:n.425-79T>A
NM_001363669.1:c.314-79T>A	NP_001350598.1:n.314-79T>A
NM_001363670.1:c.425-79T>A	NP_001350599.1:n.425-79T>A
NM_006888.5:c.422-79T>A	NP_008819.1:n.422-79T>A
NM_006888.6:c.422-79T>A MANE Select	NP_008819.1:n.422-79T>A
NM_001363669.2:c.314-79T>A	NP_001350598.1:n.314-79T>A
NM_001363670.2:c.425-79T>A	NP_001350599.1:n.425-79T>A