Canonical Allele Identifier: CA1363080252
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48583098_48583099delinsGC , CM000665.2:g.48583098_48583099delinsGC GRCh38
NC_000003.11:g.48620531_48620532delinsGC , CM000665.1:g.48620531_48620532delinsGC GRCh37
NC_000003.10:g.48595535_48595536delinsGC NCBI36
NG_007065.1:g.17154_17155delinsGC , LRG_286:g.17154_17155delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.4482+28_4482+29delinsGC MANE Select ENSP00000506558.1:n.4482+28_4482+29delins...
ENST00000328333.12:c.4482+28_4482+29delinsGC ENSP00000332371.8:n.4482+28_4482+29delins...
ENST00000487017.5:n.399+28_399+29delinsGC
NM_000094.3:c.4482+28_4482+29delinsGC , LRG_286t1:c.4482+28_4482+29delinsGC NP_000085.1:n.4482+28_4482+29delinsGC
XM_011533336.1:c.4509+28_4509+29delinsGC XP_011531638.1:n.4509+28_4509+29delinsGC
XM_011533337.1:c.4482+28_4482+29delinsGC XP_011531639.1:n.4482+28_4482+29delinsGC
XM_011533338.1:c.4509+28_4509+29delinsGC XP_011531640.1:n.4509+28_4509+29delinsGC
XM_011533339.1:c.4509+28_4509+29delinsGC XP_011531641.1:n.4509+28_4509+29delinsGC
XM_011533340.1:c.4509+28_4509+29delinsGC XP_011531642.1:n.4509+28_4509+29delinsGC
XM_011533341.1:c.4509+28_4509+29delinsGC XP_011531643.1:n.4509+28_4509+29delinsGC
XM_011533342.1:c.4509+28_4509+29delinsGC XP_011531644.1:n.4509+28_4509+29delinsGC
XR_940369.1:n.4545+28_4545+29delinsGC
XR_940370.1:n.4545+28_4545+29delinsGC
XR_940371.1:n.4545+28_4545+29delinsGC
XR_940372.1:n.4545+28_4545+29delinsGC
XR_940373.1:n.4545+28_4545+29delinsGC
XR_940374.1:n.4545+28_4545+29delinsGC
XR_940375.1:n.4545+28_4545+29delinsGC
XM_017005688.1:c.4482+28_4482+29delinsGC XP_016861177.1:n.4482+28_4482+29delinsGC
XM_017005689.1:c.4482+28_4482+29delinsGC XP_016861178.1:n.4482+28_4482+29delinsGC
XM_017005690.1:c.4482+28_4482+29delinsGC XP_016861179.1:n.4482+28_4482+29delinsGC
XM_017005691.1:c.4482+28_4482+29delinsGC XP_016861180.1:n.4482+28_4482+29delinsGC
XM_017005692.1:c.4482+28_4482+29delinsGC XP_016861181.1:n.4482+28_4482+29delinsGC
XR_001740003.1:n.4518+28_4518+29delinsGC
XR_001740004.1:n.4518+28_4518+29delinsGC
XR_001740005.1:n.4518+28_4518+29delinsGC
XR_001740006.1:n.4518+28_4518+29delinsGC
XR_001740007.1:n.4518+28_4518+29delinsGC
XR_001740008.1:n.4518+28_4518+29delinsGC
XR_001740009.1:n.4518+28_4518+29delinsGC
NM_000094.4:c.4482+28_4482+29delinsGC MANE Select NP_000085.1:n.4482+28_4482+29delinsGC