Canonical Allele Identifier: CA1363076281
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48567883C= , CM000665.2:g.48567883C= GRCh38
NC_000003.11:g.48605316C= , CM000665.1:g.48605316C= GRCh37
NC_000003.10:g.48580320C= NCBI36
NG_007065.1:g.32370G= , LRG_286:g.32370G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.7884G= MANE Select ENSP00000506558.1:p.Arg2628=
ENST00000328333.12:c.7884G= ENSP00000332371.8:p.Arg2628=
ENST00000459756.5:n.707G=
ENST00000487017.5:n.4523G=
NM_000094.3:c.7884G= , LRG_286t1:c.7884G= NP_000085.1:p.Arg2628=
XM_011533336.1:c.7911G= XP_011531638.1:p.Arg2637=
XM_011533337.1:c.7884G= XP_011531639.1:p.Arg2628=
XM_011533338.1:c.7851G= XP_011531640.1:p.Arg2617=
XR_940369.1:n.7947G=
XR_940370.1:n.7947G=
XR_940371.1:n.7947G=
XM_017005688.1:c.7824G= XP_016861177.1:p.Arg2608=
XR_001740003.1:n.7920G=
XR_001740004.1:n.7920G=
XR_001740005.1:n.7920G=
NM_000094.4:c.7884G= MANE Select NP_000085.1:p.Arg2628=