Canonical Allele Identifier: CA2378523
Gene: COL7A1 HGNC NCBI

Linked Data

dbSNP Id: rs545691941
gnomAD v2: 3-48607793-T-C
gnomAD v3: 3-48570360-T-C
gnomAD v4: 3-48570360-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48570360T>C , CM000665.2:g.48570360T>C GRCh38
NC_000003.11:g.48607793T>C , CM000665.1:g.48607793T>C GRCh37
NC_000003.10:g.48582797T>C NCBI36
NG_007065.1:g.29893A>G , LRG_286:g.29893A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.7381-26A>G MANE Select ENSP00000506558.1:n.7381-26A>G
ENST00000328333.12:c.7381-26A>G ENSP00000332371.8:n.7381-26A>G
ENST00000422991.1:c.376-26A>G ENSP00000391608.1:n.376-26A>G
ENST00000459756.5:n.82A>G
ENST00000467985.1:n.131-26A>G
ENST00000487017.5:n.4020-26A>G
NM_000094.3:c.7381-26A>G , LRG_286t1:c.7381-26A>G NP_000085.1:n.7381-26A>G
XM_011533336.1:c.7408-26A>G XP_011531638.1:n.7408-26A>G
XM_011533337.1:c.7381-26A>G XP_011531639.1:n.7381-26A>G
XM_011533338.1:c.7407+105A>G XP_011531640.1:n.7407+105A>G
XM_011533339.1:c.7408-26A>G XP_011531641.1:n.7408-26A>G
XM_011533340.1:c.7407+105A>G XP_011531642.1:n.7407+105A>G
XM_011533341.1:c.7381+105A>G XP_011531643.1:n.7381+105A>G
XM_011533342.1:c.7381+105A>G XP_011531644.1:n.7381+105A>G
XR_940369.1:n.7444-26A>G
XR_940370.1:n.7444-26A>G
XR_940371.1:n.7444-26A>G
XR_940372.1:n.7418-26A>G
XM_017005688.1:c.7380+105A>G XP_016861177.1:n.7380+105A>G
XM_017005689.1:c.7381-26A>G XP_016861178.1:n.7381-26A>G
XM_017005690.1:c.7380+105A>G XP_016861179.1:n.7380+105A>G
XM_017005691.1:c.7354+105A>G XP_016861180.1:n.7354+105A>G
XM_017005692.1:c.7354+105A>G XP_016861181.1:n.7354+105A>G
XR_001740003.1:n.7417-26A>G
XR_001740004.1:n.7417-26A>G
XR_001740005.1:n.7417-26A>G
XR_001740006.1:n.7391-26A>G
NM_000094.4:c.7381-26A>G MANE Select NP_000085.1:n.7381-26A>G