Canonical Allele Identifier: CA352687503
Gene: COL7A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1500817
ClinVar RCV Id: RCV002042662
dbSNP Id: rs1285793084
gnomAD v2: 3-48619786-C-G
gnomAD v3: 3-48582353-C-G
gnomAD v4: 3-48582353-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48582353C>G , CM000665.2:g.48582353C>G GRCh38
NC_000003.11:g.48619786C>G , CM000665.1:g.48619786C>G GRCh37
NC_000003.10:g.48594790C>G NCBI36
NG_007065.1:g.17900G>C , LRG_286:g.17900G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.4605G>C MANE Select ENSP00000506558.1:p.Glu1535Asp
ENST00000328333.12:c.4605G>C ENSP00000332371.8:p.Glu1535Asp
ENST00000487017.5:n.522G>C
NM_000094.3:c.4605G>C , LRG_286t1:c.4605G>C NP_000085.1:p.Glu1535Asp
XM_011533336.1:c.4632G>C XP_011531638.1:p.Glu1544Asp
XM_011533337.1:c.4605G>C XP_011531639.1:p.Glu1535Asp
XM_011533338.1:c.4632G>C XP_011531640.1:p.Glu1544Asp
XM_011533339.1:c.4632G>C XP_011531641.1:p.Glu1544Asp
XM_011533340.1:c.4632G>C XP_011531642.1:p.Glu1544Asp
XM_011533341.1:c.4632G>C XP_011531643.1:p.Glu1544Asp
XM_011533342.1:c.4632G>C XP_011531644.1:p.Glu1544Asp
XR_940369.1:n.4668G>C
XR_940370.1:n.4668G>C
XR_940371.1:n.4668G>C
XR_940372.1:n.4668G>C
XR_940373.1:n.4668G>C
XR_940374.1:n.4668G>C
XR_940375.1:n.4668G>C
XM_017005688.1:c.4605G>C XP_016861177.1:p.Glu1535Asp
XM_017005689.1:c.4605G>C XP_016861178.1:p.Glu1535Asp
XM_017005690.1:c.4605G>C XP_016861179.1:p.Glu1535Asp
XM_017005691.1:c.4605G>C XP_016861180.1:p.Glu1535Asp
XM_017005692.1:c.4605G>C XP_016861181.1:p.Glu1535Asp
XR_001740003.1:n.4641G>C
XR_001740004.1:n.4641G>C
XR_001740005.1:n.4641G>C
XR_001740006.1:n.4641G>C
XR_001740007.1:n.4641G>C
XR_001740008.1:n.4641G>C
XR_001740009.1:n.4641G>C
NM_000094.4:c.4605G>C MANE Select NP_000085.1:p.Glu1535Asp