Canonical Allele Identifier: CA2156375692

Gene: CLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.95254244_95254245delinsAC , CM000676.2:g.95254244_95254245delinsAC	GRCh38
NC_000014.8:g.95720581_95720582delinsAC , CM000676.1:g.95720581_95720582delinsAC	GRCh37
NC_000014.7:g.94790334_94790335delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298912.9:c.83-24112_83-24111delinsGT MANE Select	ENSP00000298912.3:n.83-24112_83-24111delinsGT
ENST00000298912.8:c.83-24112_83-24111delinsGT	ENSP00000298912.3:n.83-24112_83-24111delinsGT
ENST00000553733.1:c.83-24112_83-24111delinsGT	ENSP00000451189.1:n.83-24112_83-24111delinsGT
ENST00000555336.6:c.-123+6270_-123+6271delinsGT	ENSP00000451705.1:n.-123+6270_-123+6271delinsGT
ENST00000555615.1:c.-122-24112_-122-24111delinsGT	ENSP00000452525.1:n.-122-24112_-122-24111delinsGT
NM_024734.3:c.83-24112_83-24111delinsGT	NP_079010.2:n.83-24112_83-24111delinsGT
XM_011537158.1:c.83-24112_83-24111delinsGT	XP_011535460.1:n.83-24112_83-24111delinsGT
XM_011537159.1:c.83-24112_83-24111delinsGT	XP_011535461.1:n.83-24112_83-24111delinsGT
XR_245721.2:n.195-24112_195-24111delinsGT
XR_429330.2:n.195-24112_195-24111delinsGT
XR_429332.2:n.195-24112_195-24111delinsGT
XM_011537159.2:c.83-24112_83-24111delinsGT	XP_011535461.1:n.83-24112_83-24111delinsGT
XM_017021646.1:c.23-24112_23-24111delinsGT	XP_016877135.1:n.23-24112_23-24111delinsGT
XM_017021647.1:c.83-24112_83-24111delinsGT	XP_016877136.1:n.83-24112_83-24111delinsGT
XR_001750558.1:n.195-24112_195-24111delinsGT
NM_024734.4:c.83-24112_83-24111delinsGT MANE Select	NP_079010.2:n.83-24112_83-24111delinsGT