Canonical Allele Identifier: CA1363079547
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48582617_48582622delinsCCTTGG , CM000665.2:g.48582617_48582622delinsCCTTGG GRCh38
NC_000003.11:g.48620050_48620055delinsCCTTGG , CM000665.1:g.48620050_48620055delinsCCTTGG GRCh37
NC_000003.10:g.48595054_48595059delinsCCTTGG NCBI36
NG_007065.1:g.17631_17636delinsCCAAGG , LRG_286:g.17631_17636delinsCCAAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.4550_4555delinsCCAAGG MANE Select ENSP00000506558.1:p.Ala1517=
ENST00000328333.12:c.4550_4555delinsCCAAGG ENSP00000332371.8:p.Ala1517=
ENST00000487017.5:n.467_472delinsCCAAGG
NM_000094.3:c.4550_4555delinsCCAAGG , LRG_286t1:c.4550_4555delinsCCAAGG NP_000085.1:p.Ala1517=
XM_011533336.1:c.4577_4582delinsCCAAGG XP_011531638.1:p.Ala1526=
XM_011533337.1:c.4550_4555delinsCCAAGG XP_011531639.1:p.Ala1517=
XM_011533338.1:c.4577_4582delinsCCAAGG XP_011531640.1:p.Ala1526=
XM_011533339.1:c.4577_4582delinsCCAAGG XP_011531641.1:p.Ala1526=
XM_011533340.1:c.4577_4582delinsCCAAGG XP_011531642.1:p.Ala1526=
XM_011533341.1:c.4577_4582delinsCCAAGG XP_011531643.1:p.Ala1526=
XM_011533342.1:c.4577_4582delinsCCAAGG XP_011531644.1:p.Ala1526=
XR_940369.1:n.4613_4618delinsCCAAGG
XR_940370.1:n.4613_4618delinsCCAAGG
XR_940371.1:n.4613_4618delinsCCAAGG
XR_940372.1:n.4613_4618delinsCCAAGG
XR_940373.1:n.4613_4618delinsCCAAGG
XR_940374.1:n.4613_4618delinsCCAAGG
XR_940375.1:n.4613_4618delinsCCAAGG
XM_017005688.1:c.4550_4555delinsCCAAGG XP_016861177.1:p.Ala1517=
XM_017005689.1:c.4550_4555delinsCCAAGG XP_016861178.1:p.Ala1517=
XM_017005690.1:c.4550_4555delinsCCAAGG XP_016861179.1:p.Ala1517=
XM_017005691.1:c.4550_4555delinsCCAAGG XP_016861180.1:p.Ala1517=
XM_017005692.1:c.4550_4555delinsCCAAGG XP_016861181.1:p.Ala1517=
XR_001740003.1:n.4586_4591delinsCCAAGG
XR_001740004.1:n.4586_4591delinsCCAAGG
XR_001740005.1:n.4586_4591delinsCCAAGG
XR_001740006.1:n.4586_4591delinsCCAAGG
XR_001740007.1:n.4586_4591delinsCCAAGG
XR_001740008.1:n.4586_4591delinsCCAAGG
XR_001740009.1:n.4586_4591delinsCCAAGG
NM_000094.4:c.4550_4555delinsCCAAGG MANE Select NP_000085.1:p.Ala1517=