Canonical Allele Identifier: CA1363084062

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48578164_48578165delinsCA , CM000665.2:g.48578164_48578165delinsCA	GRCh38
NC_000003.11:g.48615597_48615598delinsCA , CM000665.1:g.48615597_48615598delinsCA	GRCh37
NC_000003.10:g.48590601_48590602delinsCA	NCBI36
NG_007065.1:g.22088_22089delinsTG , LRG_286:g.22088_22089delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.5532+156_5532+157delinsTG MANE Select	ENSP00000506558.1:n.5532+156_5532+157delinsTG
ENST00000328333.12:c.5532+156_5532+157delinsTG	ENSP00000332371.8:n.5532+156_5532+157delinsTG
ENST00000487017.5:n.1449+156_1449+157delinsTG
NM_000094.3:c.5532+156_5532+157delinsTG , LRG_286t1:c.5532+156_5532+157delinsTG	NP_000085.1:n.5532+156_5532+157delinsTG
XM_011533336.1:c.5559+156_5559+157delinsTG	XP_011531638.1:n.5559+156_5559+157delinsTG
XM_011533337.1:c.5532+156_5532+157delinsTG	XP_011531639.1:n.5532+156_5532+157delinsTG
XM_011533338.1:c.5559+156_5559+157delinsTG	XP_011531640.1:n.5559+156_5559+157delinsTG
XM_011533339.1:c.5559+156_5559+157delinsTG	XP_011531641.1:n.5559+156_5559+157delinsTG
XM_011533340.1:c.5559+156_5559+157delinsTG	XP_011531642.1:n.5559+156_5559+157delinsTG
XM_011533341.1:c.5559+156_5559+157delinsTG	XP_011531643.1:n.5559+156_5559+157delinsTG
XM_011533342.1:c.5559+156_5559+157delinsTG	XP_011531644.1:n.5559+156_5559+157delinsTG
XR_940369.1:n.5595+156_5595+157delinsTG
XR_940370.1:n.5595+156_5595+157delinsTG
XR_940371.1:n.5595+156_5595+157delinsTG
XR_940372.1:n.5595+156_5595+157delinsTG
XR_940373.1:n.5595+156_5595+157delinsTG
XR_940374.1:n.5595+156_5595+157delinsTG
XR_940375.1:n.5595+156_5595+157delinsTG
XM_017005688.1:c.5532+156_5532+157delinsTG	XP_016861177.1:n.5532+156_5532+157delinsTG
XM_017005689.1:c.5532+156_5532+157delinsTG	XP_016861178.1:n.5532+156_5532+157delinsTG
XM_017005690.1:c.5532+156_5532+157delinsTG	XP_016861179.1:n.5532+156_5532+157delinsTG
XM_017005691.1:c.5532+156_5532+157delinsTG	XP_016861180.1:n.5532+156_5532+157delinsTG
XM_017005692.1:c.5532+156_5532+157delinsTG	XP_016861181.1:n.5532+156_5532+157delinsTG
XR_001740003.1:n.5568+156_5568+157delinsTG
XR_001740004.1:n.5568+156_5568+157delinsTG
XR_001740005.1:n.5568+156_5568+157delinsTG
XR_001740006.1:n.5568+156_5568+157delinsTG
XR_001740007.1:n.5568+156_5568+157delinsTG
XR_001740008.1:n.5568+156_5568+157delinsTG
XR_001740009.1:n.5568+156_5568+157delinsTG
NM_000094.4:c.5532+156_5532+157delinsTG MANE Select	NP_000085.1:n.5532+156_5532+157delinsTG