Canonical Allele Identifier: CA1363082876

Gene: COL7A1

Linked Data

• dbSNP Id: rs2044241436

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48575582_48575604del , CM000665.2:g.48575582_48575604del	GRCh38
NC_000003.11:g.48613015_48613037del , CM000665.1:g.48613015_48613037del	GRCh37
NC_000003.10:g.48588019_48588041del	NCBI36
NG_007065.1:g.24650_24672del , LRG_286:g.24650_24672del

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.5979+23_5980-42del MANE Select	ENSP00000506558.1:n.5979+23_5980-42del
ENST00000328333.12:c.5979+23_5980-42del	ENSP00000332371.8:n.5979+23_5980-42del
ENST00000487017.5:n.1896+23_1897-42del
NM_000094.3:c.5979+23_5980-42del , LRG_286t1:c.5979+23_5980-42del	NP_000085.1:n.5979+23_5980-42del
XM_011533336.1:c.6006+23_6007-42del	XP_011531638.1:n.6006+23_6007-42del
XM_011533337.1:c.5979+23_5980-42del	XP_011531639.1:n.5979+23_5980-42del
XM_011533338.1:c.6006+23_6007-42del	XP_011531640.1:n.6006+23_6007-42del
XM_011533339.1:c.6006+23_6007-42del	XP_011531641.1:n.6006+23_6007-42del
XM_011533340.1:c.6006+23_6007-42del	XP_011531642.1:n.6006+23_6007-42del
XM_011533341.1:c.6006+23_6007-42del	XP_011531643.1:n.6006+23_6007-42del
XM_011533342.1:c.6006+23_6007-42del	XP_011531644.1:n.6006+23_6007-42del
XR_940369.1:n.6042+23_6043-42del
XR_940370.1:n.6042+23_6043-42del
XR_940371.1:n.6042+23_6043-42del
XR_940372.1:n.6042+23_6043-42del
XR_940373.1:n.6042+23_6043-42del
XR_940374.1:n.6042+23_6043-42del
XR_940375.1:n.6042+23_6043-42del
XM_017005688.1:c.5979+23_5980-42del	XP_016861177.1:n.5979+23_5980-42del
XM_017005689.1:c.5979+23_5980-42del	XP_016861178.1:n.5979+23_5980-42del
XM_017005690.1:c.5979+23_5980-42del	XP_016861179.1:n.5979+23_5980-42del
XM_017005691.1:c.5979+23_5980-42del	XP_016861180.1:n.5979+23_5980-42del
XM_017005692.1:c.5979+23_5980-42del	XP_016861181.1:n.5979+23_5980-42del
XR_001740003.1:n.6015+23_6016-42del
XR_001740004.1:n.6015+23_6016-42del
XR_001740005.1:n.6015+23_6016-42del
XR_001740006.1:n.6015+23_6016-42del
XR_001740007.1:n.6015+23_6016-42del
XR_001740008.1:n.6015+23_6016-42del
XR_001740009.1:n.6015+23_6016-42del
NM_000094.4:c.5979+23_5980-42del MANE Select	NP_000085.1:n.5979+23_5980-42del