Canonical Allele Identifier: CA1363075938
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48567710C= , CM000665.2:g.48567710C= GRCh38
NC_000003.11:g.48605143C= , CM000665.1:g.48605143C= GRCh37
NC_000003.10:g.48580147C= NCBI36
NG_007065.1:g.32543G= , LRG_286:g.32543G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.7983G= MANE Select ENSP00000506558.1:p.Met2661=
ENST00000328333.12:c.7983G= ENSP00000332371.8:p.Met2661=
ENST00000459756.5:n.806G=
ENST00000487017.5:n.4622G=
NM_000094.3:c.7983G= , LRG_286t1:c.7983G= NP_000085.1:p.Met2661=
XM_011533336.1:c.8010G= XP_011531638.1:p.Met2670=
XM_011533337.1:c.7983G= XP_011531639.1:p.Met2661=
XM_011533338.1:c.7950G= XP_011531640.1:p.Met2650=
XR_940369.1:n.8046G=
XR_940370.1:n.8046G=
XR_940371.1:n.8046G=
XM_017005688.1:c.7923G= XP_016861177.1:p.Met2641=
XR_001740003.1:n.8019G=
XR_001740004.1:n.8019G=
XR_001740005.1:n.8019G=
NM_000094.4:c.7983G= MANE Select NP_000085.1:p.Met2661=