Canonical Allele Identifier: CA1047676750
Gene: COL7A1 HGNC NCBI

Linked Data

dbSNP Id: rs2043706602
gnomAD v3: 3-48568427-A-G
gnomAD v4: 3-48568427-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48568427A>G , CM000665.2:g.48568427A>G GRCh38
NC_000003.11:g.48605860A>G , CM000665.1:g.48605860A>G GRCh37
NC_000003.10:g.48580864A>G NCBI36
NG_007065.1:g.31826T>C , LRG_286:g.31826T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.7794+72T>C MANE Select ENSP00000506558.1:n.7794+72T>C
ENST00000328333.12:c.7794+72T>C ENSP00000332371.8:n.7794+72T>C
ENST00000459756.5:n.617+72T>C
ENST00000467985.1:n.640+72T>C
ENST00000487017.5:n.4433+72T>C
NM_000094.3:c.7794+72T>C , LRG_286t1:c.7794+72T>C NP_000085.1:n.7794+72T>C
XM_011533336.1:c.7821+72T>C XP_011531638.1:n.7821+72T>C
XM_011533337.1:c.7794+72T>C XP_011531639.1:n.7794+72T>C
XM_011533338.1:c.7761+72T>C XP_011531640.1:n.7761+72T>C
XM_011533339.1:c.7821+72T>C XP_011531641.1:n.7821+72T>C
XR_940369.1:n.7857+72T>C
XR_940370.1:n.7857+72T>C
XR_940371.1:n.7857+72T>C
XR_940372.1:n.7831+72T>C
XM_017005688.1:c.7734+72T>C XP_016861177.1:n.7734+72T>C
XM_017005689.1:c.7794+72T>C XP_016861178.1:n.7794+72T>C
XR_001740003.1:n.7830+72T>C
XR_001740004.1:n.7830+72T>C
XR_001740005.1:n.7830+72T>C
XR_001740006.1:n.7804+72T>C
NM_000094.4:c.7794+72T>C MANE Select NP_000085.1:n.7794+72T>C