Canonical Allele Identifier: CA1363083537

Gene: COL7A1

Linked Data

• ClinVar Variation Id: 1047939
• ClinVar RCV Id: RCV001352703
• dbSNP Id: rs2044350714

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48576927_48576935del , CM000665.2:g.48576927_48576935del	GRCh38
NC_000003.11:g.48614360_48614368del , CM000665.1:g.48614360_48614368del	GRCh37
NC_000003.10:g.48589364_48589372del	NCBI36
NG_007065.1:g.23323_23331del , LRG_286:g.23323_23331del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.5569-11_5569-3del MANE Select	ENSP00000506558.1:n.5569-11_5569-3del
ENST00000328333.12:c.5569-11_5569-3del	ENSP00000332371.8:n.5569-11_5569-3del
ENST00000487017.5:n.1486-11_1486-3del
NM_000094.3:c.5569-11_5569-3del , LRG_286t1:c.5569-11_5569-3del	NP_000085.1:n.5569-11_5569-3del
XM_011533336.1:c.5596-11_5596-3del	XP_011531638.1:n.5596-11_5596-3del
XM_011533337.1:c.5569-11_5569-3del	XP_011531639.1:n.5569-11_5569-3del
XM_011533338.1:c.5596-11_5596-3del	XP_011531640.1:n.5596-11_5596-3del
XM_011533339.1:c.5596-11_5596-3del	XP_011531641.1:n.5596-11_5596-3del
XM_011533340.1:c.5596-11_5596-3del	XP_011531642.1:n.5596-11_5596-3del
XM_011533341.1:c.5596-11_5596-3del	XP_011531643.1:n.5596-11_5596-3del
XM_011533342.1:c.5596-11_5596-3del	XP_011531644.1:n.5596-11_5596-3del
XR_940369.1:n.5632-11_5632-3del
XR_940370.1:n.5632-11_5632-3del
XR_940371.1:n.5632-11_5632-3del
XR_940372.1:n.5632-11_5632-3del
XR_940373.1:n.5632-11_5632-3del
XR_940374.1:n.5632-11_5632-3del
XR_940375.1:n.5632-11_5632-3del
XM_017005688.1:c.5569-11_5569-3del	XP_016861177.1:n.5569-11_5569-3del
XM_017005689.1:c.5569-11_5569-3del	XP_016861178.1:n.5569-11_5569-3del
XM_017005690.1:c.5569-11_5569-3del	XP_016861179.1:n.5569-11_5569-3del
XM_017005691.1:c.5569-11_5569-3del	XP_016861180.1:n.5569-11_5569-3del
XM_017005692.1:c.5569-11_5569-3del	XP_016861181.1:n.5569-11_5569-3del
XR_001740003.1:n.5605-11_5605-3del
XR_001740004.1:n.5605-11_5605-3del
XR_001740005.1:n.5605-11_5605-3del
XR_001740006.1:n.5605-11_5605-3del
XR_001740007.1:n.5605-11_5605-3del
XR_001740008.1:n.5605-11_5605-3del
XR_001740009.1:n.5605-11_5605-3del
NM_000094.4:c.5569-11_5569-3del MANE Select	NP_000085.1:n.5569-11_5569-3del