Canonical Allele Identifier: CA265912359
Gene: CLMN HGNC NCBI

Linked Data

dbSNP Id: rs1187614

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.95205534G>T , CM000676.2:g.95205534G>T GRCh38
NC_000014.8:g.95671871G>T , CM000676.1:g.95671871G>T GRCh37
NC_000014.7:g.94741624G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000298912.9:c.886-1071C>A MANE Select ENSP00000298912.3:n.886-1071C>A
ENST00000298912.8:c.886-1071C>A ENSP00000298912.3:n.886-1071C>A
ENST00000556454.1:n.250-1071C>A
NM_024734.3:c.886-1071C>A NP_079010.2:n.886-1071C>A
XM_011537158.1:c.886-1071C>A XP_011535460.1:n.886-1071C>A
XM_011537159.1:c.886-1071C>A XP_011535461.1:n.886-1071C>A
XR_245721.2:n.998-1071C>A
XR_429330.2:n.998-1071C>A
XR_429332.2:n.998-1071C>A
XM_011537159.2:c.886-1071C>A XP_011535461.1:n.886-1071C>A
XM_017021646.1:c.826-1071C>A XP_016877135.1:n.826-1071C>A
XM_017021647.1:c.886-1071C>A XP_016877136.1:n.886-1071C>A
XR_001750558.1:n.998-1071C>A
NM_024734.4:c.886-1071C>A MANE Select NP_079010.2:n.886-1071C>A