Canonical Allele Identifier: CA1363075509
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48567377C= , CM000665.2:g.48567377C= GRCh38
NC_000003.11:g.48604810C= , CM000665.1:g.48604810C= GRCh37
NC_000003.10:g.48579814C= NCBI36
NG_007065.1:g.32876G= , LRG_286:g.32876G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.8047-187G= MANE Select ENSP00000506558.1:n.8047-187G=
ENST00000328333.12:c.8047-187G= ENSP00000332371.8:n.8047-187G=
ENST00000487017.5:n.4686-187G=
NM_000094.3:c.8047-187G= , LRG_286t1:c.8047-187G= NP_000085.1:n.8047-187G=
XM_011533336.1:c.8074-187G= XP_011531638.1:n.8074-187G=
XM_011533337.1:c.8047-187G= XP_011531639.1:n.8047-187G=
XM_011533338.1:c.8014-187G= XP_011531640.1:n.8014-187G=
XR_940369.1:n.8110-187G=
XR_940370.1:n.8110-187G=
XR_940371.1:n.8110-187G=
XM_017005688.1:c.7987-187G= XP_016861177.1:n.7987-187G=
XR_001740003.1:n.8083-187G=
XR_001740004.1:n.8083-187G=
XR_001740005.1:n.8083-187G=
NM_000094.4:c.8047-187G= MANE Select NP_000085.1:n.8047-187G=