Canonical Allele Identifier: CA2580069973
Gene: COL7A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1676653
ClinVar RCV Id: RCV002277089
dbSNP Id: rs2107671950

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48575107_48575108delinsTT , CM000665.2:g.48575107_48575108delinsTT GRCh38
NC_000003.11:g.48612540_48612541delinsTT , CM000665.1:g.48612540_48612541delinsTT GRCh37
NC_000003.10:g.48587544_48587545delinsTT NCBI36
NG_007065.1:g.25145_25146delinsAA , LRG_286:g.25145_25146delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.6235_6236delinsAA MANE Select ENSP00000506558.1:p.Gly2079Lys
ENST00000328333.12:c.6235_6236delinsAA ENSP00000332371.8:p.Gly2079Lys
ENST00000487017.5:n.2152_2153delinsAA
NM_000094.3:c.6235_6236delinsAA , LRG_286t1:c.6235_6236delinsAA NP_000085.1:p.Gly2079Lys
XM_011533336.1:c.6262_6263delinsAA XP_011531638.1:p.Gly2088Lys
XM_011533337.1:c.6235_6236delinsAA XP_011531639.1:p.Gly2079Lys
XM_011533338.1:c.6262_6263delinsAA XP_011531640.1:p.Gly2088Lys
XM_011533339.1:c.6262_6263delinsAA XP_011531641.1:p.Gly2088Lys
XM_011533340.1:c.6262_6263delinsAA XP_011531642.1:p.Gly2088Lys
XM_011533341.1:c.6262_6263delinsAA XP_011531643.1:p.Gly2088Lys
XM_011533342.1:c.6262_6263delinsAA XP_011531644.1:p.Gly2088Lys
XR_940369.1:n.6298_6299delinsAA
XR_940370.1:n.6298_6299delinsAA
XR_940371.1:n.6298_6299delinsAA
XR_940372.1:n.6298_6299delinsAA
XR_940373.1:n.6298_6299delinsAA
XR_940374.1:n.6298_6299delinsAA
XR_940375.1:n.6236_6237delinsAA
XM_017005688.1:c.6235_6236delinsAA XP_016861177.1:p.Gly2079Lys
XM_017005689.1:c.6235_6236delinsAA XP_016861178.1:p.Gly2079Lys
XM_017005690.1:c.6235_6236delinsAA XP_016861179.1:p.Gly2079Lys
XM_017005691.1:c.6235_6236delinsAA XP_016861180.1:p.Gly2079Lys
XM_017005692.1:c.6235_6236delinsAA XP_016861181.1:p.Gly2079Lys
XR_001740003.1:n.6271_6272delinsAA
XR_001740004.1:n.6271_6272delinsAA
XR_001740005.1:n.6271_6272delinsAA
XR_001740006.1:n.6271_6272delinsAA
XR_001740007.1:n.6271_6272delinsAA
XR_001740008.1:n.6271_6272delinsAA
XR_001740009.1:n.6209_6210delinsAA
NM_000094.4:c.6235_6236delinsAA MANE Select NP_000085.1:p.Gly2079Lys