Canonical Allele Identifier: CA2841666935
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48566203dup , CM000665.2:g.48566203dup GRCh38
NC_000003.11:g.48603636dup , CM000665.1:g.48603636dup GRCh37
NC_000003.10:g.48578640dup NCBI36
NG_007065.1:g.34053dup , LRG_286:g.34053dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.8407+67dup MANE Select ENSP00000506558.1:n.8407+67dup
ENST00000328333.12:c.8407+67dup ENSP00000332371.8:n.8407+67dup
ENST00000487017.5:n.5046+67dup
NM_000094.3:c.8407+67dup , LRG_286t1:c.8407+67dup NP_000085.1:n.8407+67dup
XM_011533336.1:c.8434+67dup XP_011531638.1:n.8434+67dup
XM_011533337.1:c.8407+67dup XP_011531639.1:n.8407+67dup
XM_011533338.1:c.8374+67dup XP_011531640.1:n.8374+67dup
XR_940369.1:n.8470+67dup
XR_940370.1:n.8470+67dup
XR_940371.1:n.8470+67dup
XM_017005688.1:c.8347+67dup XP_016861177.1:n.8347+67dup
XR_001740003.1:n.8443+67dup
XR_001740004.1:n.8443+67dup
XR_001740005.1:n.8443+67dup
NM_000094.4:c.8407+67dup MANE Select NP_000085.1:n.8407+67dup