Canonical Allele Identifier: CA2665620057
Gene: COL7A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48568748_48568759dup , CM000665.2:g.48568748_48568759dup GRCh38
NC_000003.11:g.48606181_48606192dup , CM000665.1:g.48606181_48606192dup GRCh37
NC_000003.10:g.48581185_48581196dup NCBI36
NG_007065.1:g.31498_31509dup , LRG_286:g.31498_31509dup

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.7758+29_7758+40dup MANE Select ENSP00000506558.1:n.7758+29_7758+40dup
ENST00000328333.12:c.7758+29_7758+40dup ENSP00000332371.8:n.7758+29_7758+40dup
ENST00000459756.5:n.581+29_581+40dup
ENST00000467985.1:n.604+29_604+40dup
ENST00000487017.5:n.4397+29_4397+40dup
NM_000094.3:c.7758+29_7758+40dup , LRG_286t1:c.7758+29_7758+40dup NP_000085.1:n.7758+29_7758+40dup
XM_011533336.1:c.7785+29_7785+40dup XP_011531638.1:n.7785+29_7785+40dup
XM_011533337.1:c.7758+29_7758+40dup XP_011531639.1:n.7758+29_7758+40dup
XM_011533338.1:c.7725+29_7725+40dup XP_011531640.1:n.7725+29_7725+40dup
XM_011533339.1:c.7785+29_7785+40dup XP_011531641.1:n.7785+29_7785+40dup
XR_940369.1:n.7821+29_7821+40dup
XR_940370.1:n.7821+29_7821+40dup
XR_940371.1:n.7821+29_7821+40dup
XR_940372.1:n.7795+29_7795+40dup
XM_017005688.1:c.7698+29_7698+40dup XP_016861177.1:n.7698+29_7698+40dup
XM_017005689.1:c.7758+29_7758+40dup XP_016861178.1:n.7758+29_7758+40dup
XR_001740003.1:n.7794+29_7794+40dup
XR_001740004.1:n.7794+29_7794+40dup
XR_001740005.1:n.7794+29_7794+40dup
XR_001740006.1:n.7768+29_7768+40dup
NM_000094.4:c.7758+29_7758+40dup MANE Select NP_000085.1:n.7758+29_7758+40dup