Canonical Allele Identifier: CA1387934101
Gene: COL8A1 HGNC NCBI

Linked Data

dbSNP Id: rs1938734593

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.99677459del , CM000665.2:g.99677459del GRCh38
NC_000003.11:g.99396303del , CM000665.1:g.99396303del GRCh37
NC_000003.10:g.100878993del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652472.1:c.-129+38795del MANE Select ENSP00000498483.1:n.-129+38795del
ENST00000261037.7:c.-129+1738del ENSP00000261037.3:n.-129+1738del
ENST00000273342.8:c.-129+38795del ENSP00000273342.3:n.-129+38795del
ENST00000452013.5:c.-129+38795del ENSP00000387589.1:n.-129+38795del
ENST00000463753.5:n.253-292del
ENST00000474648.5:n.252+1738del
ENST00000483969.5:n.252+1738del
ENST00000621757.1:c.-298-13940del ENSP00000482679.1:n.-298-13940del
NM_001850.4:c.-129+1738del NP_001841.2:n.-129+1738del
NM_020351.3:c.-129+38795del NP_065084.2:n.-129+38795del
NM_020351.4:c.-129+38795del MANE Select NP_065084.2:n.-129+38795del
NM_001850.5:c.-129+1738del NP_001841.2:n.-129+1738del