Canonical Allele Identifier: CA2154484207

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404507C= , CM000676.2:g.90404507C=	GRCh38
NC_000014.8:g.90870851C= , CM000676.1:g.90870851C=	GRCh37
NC_000014.7:g.89940604C=	NCBI36
NG_013338.1:g.12525C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.414C= MANE Select	ENSP00000349467.4:p.Asn138=
ENST00000447653.8:c.306C=	ENSP00000403491.4:p.Asn102=
ENST00000659177.1:c.306C=	ENSP00000499421.1:p.Asn102=
ENST00000663135.1:c.306C=	ENSP00000499498.1:p.Asn102=
ENST00000356978.8:c.414C=	ENSP00000349467.4:p.Asn138=
ENST00000447653.7:c.417C=	ENSP00000403491.3:p.Asn139=
ENST00000544280.6:c.306C=	ENSP00000442853.2:p.Asn102=
ENST00000553422.1:c.286C=	ENSP00000450425.1:n.286C=
ENST00000553542.5:c.306C=	ENSP00000450829.1:p.Asn102=
ENST00000553630.1:c.*55C=	ENSP00000451646.1:n.*55C=
ENST00000553964.5:n.2544C=
ENST00000554296.1:n.466C=
ENST00000556721.1:n.340C=
ENST00000626705.2:c.216C=	ENSP00000486402.1:p.Asn72=
NM_006888.4:c.414C=	NP_008819.1:p.Asn138=
XM_006720258.2:c.417C=	XP_006720321.1:p.Asn139=
NM_001363669.1:c.306C=	NP_001350598.1:p.Asn102=
NM_001363670.1:c.417C=	NP_001350599.1:p.Asn139=
NM_006888.5:c.414C=	NP_008819.1:p.Asn138=
NM_006888.6:c.414C= MANE Select	NP_008819.1:p.Asn138=
NM_001363669.2:c.306C=	NP_001350598.1:p.Asn102=
NM_001363670.2:c.417C=	NP_001350599.1:p.Asn139=