Canonical Allele Identifier: CA2156398195

Gene: CLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.95298244G= , CM000676.2:g.95298244G=	GRCh38
NC_000014.8:g.95764581G= , CM000676.1:g.95764581G=	GRCh37
NC_000014.7:g.94834334G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000298912.9:c.82+21467C= MANE Select	ENSP00000298912.3:n.82+21467C=
ENST00000298912.8:c.82+21467C=	ENSP00000298912.3:n.82+21467C=
ENST00000553733.1:c.82+21467C=	ENSP00000451189.1:n.82+21467C=
ENST00000555615.1:c.-123+9270C=	ENSP00000452525.1:n.-123+9270C=
NM_024734.3:c.82+21467C=	NP_079010.2:n.82+21467C=
XM_011537158.1:c.82+21467C=	XP_011535460.1:n.82+21467C=
XM_011537159.1:c.82+21467C=	XP_011535461.1:n.82+21467C=
XR_245721.2:n.194+21467C=
XR_429330.2:n.194+21467C=
XR_429332.2:n.194+21467C=
XM_011537159.2:c.82+21467C=	XP_011535461.1:n.82+21467C=
XM_017021646.1:c.22+20995C=	XP_016877135.1:n.22+20995C=
XM_017021647.1:c.82+21467C=	XP_016877136.1:n.82+21467C=
XR_001750558.1:n.194+21467C=
NM_024734.4:c.82+21467C= MANE Select	NP_079010.2:n.82+21467C=