Canonical Allele Identifier: CA1363080048
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48566201G= , CM000665.2:g.48566201G= GRCh38
NC_000003.11:g.48603634G= , CM000665.1:g.48603634G= GRCh37
NC_000003.10:g.48578638G= NCBI36
NG_007065.1:g.34052C= , LRG_286:g.34052C=

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.8407+66C= MANE Select ENSP00000506558.1:n.8407+66C=
ENST00000328333.12:c.8407+66C= ENSP00000332371.8:n.8407+66C=
ENST00000487017.5:n.5046+66C=
NM_000094.3:c.8407+66C= , LRG_286t1:c.8407+66C= NP_000085.1:n.8407+66C=
XM_011533336.1:c.8434+66C= XP_011531638.1:n.8434+66C=
XM_011533337.1:c.8407+66C= XP_011531639.1:n.8407+66C=
XM_011533338.1:c.8374+66C= XP_011531640.1:n.8374+66C=
XR_940369.1:n.8470+66C=
XR_940370.1:n.8470+66C=
XR_940371.1:n.8470+66C=
XM_017005688.1:c.8347+66C= XP_016861177.1:n.8347+66C=
XR_001740003.1:n.8443+66C=
XR_001740004.1:n.8443+66C=
XR_001740005.1:n.8443+66C=
NM_000094.4:c.8407+66C= MANE Select NP_000085.1:n.8407+66C=