Canonical Allele Identifier: CA2838407590
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48566232dup , CM000665.2:g.48566232dup GRCh38
NC_000003.11:g.48603665dup , CM000665.1:g.48603665dup GRCh37
NC_000003.10:g.48578669dup NCBI36
NG_007065.1:g.34024dup , LRG_286:g.34024dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.8407+38dup MANE Select ENSP00000506558.1:n.8407+38dup
ENST00000328333.12:c.8407+38dup ENSP00000332371.8:n.8407+38dup
ENST00000487017.5:n.5046+38dup
NM_000094.3:c.8407+38dup , LRG_286t1:c.8407+38dup NP_000085.1:n.8407+38dup
XM_011533336.1:c.8434+38dup XP_011531638.1:n.8434+38dup
XM_011533337.1:c.8407+38dup XP_011531639.1:n.8407+38dup
XM_011533338.1:c.8374+38dup XP_011531640.1:n.8374+38dup
XR_940369.1:n.8470+38dup
XR_940370.1:n.8470+38dup
XR_940371.1:n.8470+38dup
XM_017005688.1:c.8347+38dup XP_016861177.1:n.8347+38dup
XR_001740003.1:n.8443+38dup
XR_001740004.1:n.8443+38dup
XR_001740005.1:n.8443+38dup
NM_000094.4:c.8407+38dup MANE Select NP_000085.1:n.8407+38dup