Canonical Allele Identifier: CA1363075848
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48567653A= , CM000665.2:g.48567653A= GRCh38
NC_000003.11:g.48605086A= , CM000665.1:g.48605086A= GRCh37
NC_000003.10:g.48580090A= NCBI36
NG_007065.1:g.32600T= , LRG_286:g.32600T=

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.7984-17T= MANE Select ENSP00000506558.1:n.7984-17T=
ENST00000328333.12:c.7984-17T= ENSP00000332371.8:n.7984-17T=
ENST00000487017.5:n.4623-17T=
NM_000094.3:c.7984-17T= , LRG_286t1:c.7984-17T= NP_000085.1:n.7984-17T=
XM_011533336.1:c.8011-17T= XP_011531638.1:n.8011-17T=
XM_011533337.1:c.7984-17T= XP_011531639.1:n.7984-17T=
XM_011533338.1:c.7951-17T= XP_011531640.1:n.7951-17T=
XR_940369.1:n.8047-17T=
XR_940370.1:n.8047-17T=
XR_940371.1:n.8047-17T=
XM_017005688.1:c.7924-17T= XP_016861177.1:n.7924-17T=
XR_001740003.1:n.8020-17T=
XR_001740004.1:n.8020-17T=
XR_001740005.1:n.8020-17T=
NM_000094.4:c.7984-17T= MANE Select NP_000085.1:n.7984-17T=