Canonical Allele Identifier: CA1363076028
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48567742G= , CM000665.2:g.48567742G= GRCh38
NC_000003.11:g.48605175G= , CM000665.1:g.48605175G= GRCh37
NC_000003.10:g.48580179G= NCBI36
NG_007065.1:g.32511C= , LRG_286:g.32511C=

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.7951C= MANE Select ENSP00000506558.1:p.Arg2651=
ENST00000328333.12:c.7951C= ENSP00000332371.8:p.Arg2651=
ENST00000459756.5:n.774C=
ENST00000487017.5:n.4590C=
NM_000094.3:c.7951C= , LRG_286t1:c.7951C= NP_000085.1:p.Arg2651=
XM_011533336.1:c.7978C= XP_011531638.1:p.Arg2660=
XM_011533337.1:c.7951C= XP_011531639.1:p.Arg2651=
XM_011533338.1:c.7918C= XP_011531640.1:p.Arg2640=
XR_940369.1:n.8014C=
XR_940370.1:n.8014C=
XR_940371.1:n.8014C=
XM_017005688.1:c.7891C= XP_016861177.1:p.Arg2631=
XR_001740003.1:n.7987C=
XR_001740004.1:n.7987C=
XR_001740005.1:n.7987C=
NM_000094.4:c.7951C= MANE Select NP_000085.1:p.Arg2651=