Canonical Allele Identifier: CA10616858
Gene: COL7A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 345808
ClinVar RCV Id: RCV000295335
dbSNP Id: rs886058632

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48570307G>T , CM000665.2:g.48570307G>T GRCh38
NC_000003.11:g.48607740G>T , CM000665.1:g.48607740G>T GRCh37
NC_000003.10:g.48582744G>T NCBI36
NG_007065.1:g.29946C>A , LRG_286:g.29946C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.7408C>A MANE Select ENSP00000506558.1:p.Pro2470Thr
ENST00000328333.12:c.7408C>A ENSP00000332371.8:p.Pro2470Thr
ENST00000422991.1:c.403C>A ENSP00000391608.1:p.Pro135Thr
ENST00000459756.5:n.135C>A
ENST00000467985.1:n.158C>A
ENST00000487017.5:n.4047C>A
NM_000094.3:c.7408C>A , LRG_286t1:c.7408C>A NP_000085.1:p.Pro2470Thr
XM_011533336.1:c.7435C>A XP_011531638.1:p.Pro2479Thr
XM_011533337.1:c.7408C>A XP_011531639.1:p.Pro2470Thr
XM_011533338.1:c.7408-129C>A XP_011531640.1:n.7408-129C>A
XM_011533339.1:c.7435C>A XP_011531641.1:p.Pro2479Thr
XM_011533340.1:c.7408-55C>A XP_011531642.1:n.7408-55C>A
XM_011533341.1:c.7382-55C>A XP_011531643.1:n.7382-55C>A
XM_011533342.1:c.7382-129C>A XP_011531644.1:n.7382-129C>A
XR_940369.1:n.7471C>A
XR_940370.1:n.7471C>A
XR_940371.1:n.7471C>A
XR_940372.1:n.7445C>A
XM_017005688.1:c.7381-129C>A XP_016861177.1:n.7381-129C>A
XM_017005689.1:c.7408C>A XP_016861178.1:p.Pro2470Thr
XM_017005690.1:c.7381-55C>A XP_016861179.1:n.7381-55C>A
XM_017005691.1:c.7355-55C>A XP_016861180.1:n.7355-55C>A
XM_017005692.1:c.7355-129C>A XP_016861181.1:n.7355-129C>A
XR_001740003.1:n.7444C>A
XR_001740004.1:n.7444C>A
XR_001740005.1:n.7444C>A
XR_001740006.1:n.7418C>A
NM_000094.4:c.7408C>A MANE Select NP_000085.1:p.Pro2470Thr