Canonical Allele Identifier: CA1363077724
Gene: COL7A1 HGNC NCBI

Linked Data

dbSNP Id: rs2043742764

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48568819del , CM000665.2:g.48568819del GRCh38
NC_000003.11:g.48606252del , CM000665.1:g.48606252del GRCh37
NC_000003.10:g.48581256del NCBI36
NG_007065.1:g.31436del , LRG_286:g.31436del

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.7725del MANE Select ENSP00000506558.1:p.Leu2576CysfsTer?
ENST00000328333.12:c.7725del ENSP00000332371.8:p.Leu2576CysfsTer?
ENST00000459756.5:n.548del
ENST00000467985.1:n.571del
ENST00000487017.5:n.4364del
NM_000094.3:c.7725del , LRG_286t1:c.7725del NP_000085.1:p.Leu2576CysfsTer?
XM_011533336.1:c.7752del XP_011531638.1:p.Leu2585CysfsTer?
XM_011533337.1:c.7725del XP_011531639.1:p.Leu2576CysfsTer?
XM_011533338.1:c.7692del XP_011531640.1:p.Leu2565CysfsTer?
XM_011533339.1:c.7752del XP_011531641.1:p.Leu2585CysfsTer?
XR_940369.1:n.7788del
XR_940370.1:n.7788del
XR_940371.1:n.7788del
XR_940372.1:n.7762del
XM_017005688.1:c.7665del XP_016861177.1:p.Leu2556CysfsTer?
XM_017005689.1:c.7725del XP_016861178.1:p.Leu2576CysfsTer?
XR_001740003.1:n.7761del
XR_001740004.1:n.7761del
XR_001740005.1:n.7761del
XR_001740006.1:n.7735del
NM_000094.4:c.7725del MANE Select NP_000085.1:p.Leu2576CysfsTer?