Canonical Allele Identifier: CA1363075702
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48567582C= , CM000665.2:g.48567582C= GRCh38
NC_000003.11:g.48605015C= , CM000665.1:g.48605015C= GRCh37
NC_000003.10:g.48580019C= NCBI36
NG_007065.1:g.32671G= , LRG_286:g.32671G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.8038G= MANE Select ENSP00000506558.1:p.Gly2680=
ENST00000328333.12:c.8038G= ENSP00000332371.8:p.Gly2680=
ENST00000487017.5:n.4677G=
NM_000094.3:c.8038G= , LRG_286t1:c.8038G= NP_000085.1:p.Gly2680=
XM_011533336.1:c.8065G= XP_011531638.1:p.Gly2689=
XM_011533337.1:c.8038G= XP_011531639.1:p.Gly2680=
XM_011533338.1:c.8005G= XP_011531640.1:p.Gly2669=
XR_940369.1:n.8101G=
XR_940370.1:n.8101G=
XR_940371.1:n.8101G=
XM_017005688.1:c.7978G= XP_016861177.1:p.Gly2660=
XR_001740003.1:n.8074G=
XR_001740004.1:n.8074G=
XR_001740005.1:n.8074G=
NM_000094.4:c.8038G= MANE Select NP_000085.1:p.Gly2680=