Canonical Allele Identifier: CA1363079480
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48570236G= , CM000665.2:g.48570236G= GRCh38
NC_000003.11:g.48607669G= , CM000665.1:g.48607669G= GRCh37
NC_000003.10:g.48582673G= NCBI36
NG_007065.1:g.30017C= , LRG_286:g.30017C=

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.7440+39C= MANE Select ENSP00000506558.1:n.7440+39C=
ENST00000328333.12:c.7440+39C= ENSP00000332371.8:n.7440+39C=
ENST00000422991.1:c.435+39C= ENSP00000391608.1:n.435+39C=
ENST00000459756.5:n.206C=
ENST00000467985.1:n.229C=
ENST00000487017.5:n.4079+39C=
NM_000094.3:c.7440+39C= , LRG_286t1:c.7440+39C= NP_000085.1:n.7440+39C=
XM_011533336.1:c.7467+39C= XP_011531638.1:n.7467+39C=
XM_011533337.1:c.7440+39C= XP_011531639.1:n.7440+39C=
XM_011533338.1:c.7408-58C= XP_011531640.1:n.7408-58C=
XM_011533339.1:c.7467+39C= XP_011531641.1:n.7467+39C=
XM_011533340.1:c.7424C= XP_011531642.1:p.Pro2475=
XM_011533341.1:c.7398C= XP_011531643.1:p.Ser2466=
XM_011533342.1:c.7382-58C= XP_011531644.1:n.7382-58C=
XR_940369.1:n.7503+39C=
XR_940370.1:n.7503+39C=
XR_940371.1:n.7503+39C=
XR_940372.1:n.7477+39C=
XM_017005688.1:c.7381-58C= XP_016861177.1:n.7381-58C=
XM_017005689.1:c.7440+39C= XP_016861178.1:n.7440+39C=
XM_017005690.1:c.7397C= XP_016861179.1:p.Pro2466=
XM_017005691.1:c.7371C= XP_016861180.1:p.Ser2457=
XM_017005692.1:c.7355-58C= XP_016861181.1:n.7355-58C=
XR_001740003.1:n.7476+39C=
XR_001740004.1:n.7476+39C=
XR_001740005.1:n.7476+39C=
XR_001740006.1:n.7450+39C=
NM_000094.4:c.7440+39C= MANE Select NP_000085.1:n.7440+39C=