Canonical Allele Identifier: CA1139771298
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48575073_48575074del , CM000665.2:g.48575073_48575074del GRCh38
NC_000003.11:g.48612506_48612507del , CM000665.1:g.48612506_48612507del GRCh37
NC_000003.10:g.48587510_48587511del NCBI36
NG_007065.1:g.25179_25180del , LRG_286:g.25179_25180del

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.6269_6270del MANE Select ENSP00000506558.1:p.Pro2090ArgfsTer8
ENST00000328333.12:c.6269_6270del ENSP00000332371.8:p.Pro2090ArgfsTer8
ENST00000487017.5:n.2186_2187del
NM_000094.3:c.6269_6270del , LRG_286t1:c.6269_6270del NP_000085.1:p.Pro2090ArgfsTer8
XM_011533336.1:c.6296_6297del XP_011531638.1:p.Pro2099ArgfsTer8
XM_011533337.1:c.6269_6270del XP_011531639.1:p.Pro2090ArgfsTer8
XM_011533338.1:c.6296_6297del XP_011531640.1:p.Pro2099ArgfsTer8
XM_011533339.1:c.6296_6297del XP_011531641.1:p.Pro2099ArgfsTer8
XM_011533340.1:c.6296_6297del XP_011531642.1:p.Pro2099ArgfsTer8
XM_011533341.1:c.6296_6297del XP_011531643.1:p.Pro2099ArgfsTer8
XM_011533342.1:c.6296_6297del XP_011531644.1:p.Pro2099ArgfsTer8
XR_940369.1:n.6332_6333del
XR_940370.1:n.6332_6333del
XR_940371.1:n.6332_6333del
XR_940372.1:n.6332_6333del
XR_940373.1:n.6332_6333del
XR_940374.1:n.6332_6333del
XR_940375.1:n.6270_6271del
XM_017005688.1:c.6269_6270del XP_016861177.1:p.Pro2090ArgfsTer8
XM_017005689.1:c.6269_6270del XP_016861178.1:p.Pro2090ArgfsTer8
XM_017005690.1:c.6269_6270del XP_016861179.1:p.Pro2090ArgfsTer8
XM_017005691.1:c.6269_6270del XP_016861180.1:p.Pro2090ArgfsTer8
XM_017005692.1:c.6269_6270del XP_016861181.1:p.Pro2090ArgfsTer8
XR_001740003.1:n.6305_6306del
XR_001740004.1:n.6305_6306del
XR_001740005.1:n.6305_6306del
XR_001740006.1:n.6305_6306del
XR_001740007.1:n.6305_6306del
XR_001740008.1:n.6305_6306del
XR_001740009.1:n.6243_6244del
NM_000094.4:c.6269_6270del MANE Select NP_000085.1:p.Pro2090ArgfsTer8