Canonical Allele Identifier: CA1363079083
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48565497C= , CM000665.2:g.48565497C= GRCh38
NC_000003.11:g.48602930C= , CM000665.1:g.48602930C= GRCh37
NC_000003.10:g.48577934C= NCBI36
NG_007065.1:g.34756G= , LRG_286:g.34756G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.8441-1G= MANE Select ENSP00000506558.1:n.8441-1G=
ENST00000328333.12:c.8441-1G= ENSP00000332371.8:n.8441-1G=
ENST00000487017.5:n.5080-1G=
NM_000094.3:c.8441-1G= , LRG_286t1:c.8441-1G= NP_000085.1:n.8441-1G=
XM_011533336.1:c.8468-1G= XP_011531638.1:n.8468-1G=
XM_011533337.1:c.8441-1G= XP_011531639.1:n.8441-1G=
XM_011533338.1:c.8408-1G= XP_011531640.1:n.8408-1G=
XR_940369.1:n.8504-1G=
XR_940370.1:n.8504-1G=
XR_940371.1:n.8504-1G=
XM_017005688.1:c.8381-1G= XP_016861177.1:n.8381-1G=
XR_001740003.1:n.8477-1G=
XR_001740004.1:n.8477-1G=
XR_001740005.1:n.8477-1G=
NM_000094.4:c.8441-1G= MANE Select NP_000085.1:n.8441-1G=