Canonical Allele Identifier: CA1363075693
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48567578G= , CM000665.2:g.48567578G= GRCh38
NC_000003.11:g.48605011G= , CM000665.1:g.48605011G= GRCh37
NC_000003.10:g.48580015G= NCBI36
NG_007065.1:g.32675C= , LRG_286:g.32675C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.8042C= MANE Select ENSP00000506558.1:p.Pro2681=
ENST00000328333.12:c.8042C= ENSP00000332371.8:p.Pro2681=
ENST00000487017.5:n.4681C=
NM_000094.3:c.8042C= , LRG_286t1:c.8042C= NP_000085.1:p.Pro2681=
XM_011533336.1:c.8069C= XP_011531638.1:p.Pro2690=
XM_011533337.1:c.8042C= XP_011531639.1:p.Pro2681=
XM_011533338.1:c.8009C= XP_011531640.1:p.Pro2670=
XR_940369.1:n.8105C=
XR_940370.1:n.8105C=
XR_940371.1:n.8105C=
XM_017005688.1:c.7982C= XP_016861177.1:p.Pro2661=
XR_001740003.1:n.8078C=
XR_001740004.1:n.8078C=
XR_001740005.1:n.8078C=
NM_000094.4:c.8042C= MANE Select NP_000085.1:p.Pro2681=