Canonical Allele Identifier: CA1363082936

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48575699_48575713delinsCTACCAGAGCTCTCA , CM000665.2:g.48575699_48575713delinsCTACCAGAGCTCTCA	GRCh38
NC_000003.11:g.48613132_48613146delinsCTACCAGAGCTCTCA , CM000665.1:g.48613132_48613146delinsCTACCAGAGCTCTCA	GRCh37
NC_000003.10:g.48588136_48588150delinsCTACCAGAGCTCTCA	NCBI36
NG_007065.1:g.24540_24554delinsTGAGAGCTCTGGTAG , LRG_286:g.24540_24554delinsTGAGAGCTCTGGTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.5892_5906delinsTGAGAGCTCTGGTAG MANE Select	ENSP00000506558.1:p.Asp1964=
ENST00000328333.12:c.5892_5906delinsTGAGAGCTCTGGTAG	ENSP00000332371.8:p.Asp1964=
ENST00000487017.5:n.1809_1823delinsTGAGAGCTCTGGTAG
NM_000094.3:c.5892_5906delinsTGAGAGCTCTGGTAG , LRG_286t1:c.5892_5906delinsTGAGAGCTCTGGTAG	NP_000085.1:p.Asp1964=
XM_011533336.1:c.5919_5933delinsTGAGAGCTCTGGTAG	XP_011531638.1:p.Asp1973=
XM_011533337.1:c.5892_5906delinsTGAGAGCTCTGGTAG	XP_011531639.1:p.Asp1964=
XM_011533338.1:c.5919_5933delinsTGAGAGCTCTGGTAG	XP_011531640.1:p.Asp1973=
XM_011533339.1:c.5919_5933delinsTGAGAGCTCTGGTAG	XP_011531641.1:p.Asp1973=
XM_011533340.1:c.5919_5933delinsTGAGAGCTCTGGTAG	XP_011531642.1:p.Asp1973=
XM_011533341.1:c.5919_5933delinsTGAGAGCTCTGGTAG	XP_011531643.1:p.Asp1973=
XM_011533342.1:c.5919_5933delinsTGAGAGCTCTGGTAG	XP_011531644.1:p.Asp1973=
XR_940369.1:n.5955_5969delinsTGAGAGCTCTGGTAG
XR_940370.1:n.5955_5969delinsTGAGAGCTCTGGTAG
XR_940371.1:n.5955_5969delinsTGAGAGCTCTGGTAG
XR_940372.1:n.5955_5969delinsTGAGAGCTCTGGTAG
XR_940373.1:n.5955_5969delinsTGAGAGCTCTGGTAG
XR_940374.1:n.5955_5969delinsTGAGAGCTCTGGTAG
XR_940375.1:n.5955_5969delinsTGAGAGCTCTGGTAG
XM_017005688.1:c.5892_5906delinsTGAGAGCTCTGGTAG	XP_016861177.1:p.Asp1964=
XM_017005689.1:c.5892_5906delinsTGAGAGCTCTGGTAG	XP_016861178.1:p.Asp1964=
XM_017005690.1:c.5892_5906delinsTGAGAGCTCTGGTAG	XP_016861179.1:p.Asp1964=
XM_017005691.1:c.5892_5906delinsTGAGAGCTCTGGTAG	XP_016861180.1:p.Asp1964=
XM_017005692.1:c.5892_5906delinsTGAGAGCTCTGGTAG	XP_016861181.1:p.Asp1964=
XR_001740003.1:n.5928_5942delinsTGAGAGCTCTGGTAG
XR_001740004.1:n.5928_5942delinsTGAGAGCTCTGGTAG
XR_001740005.1:n.5928_5942delinsTGAGAGCTCTGGTAG
XR_001740006.1:n.5928_5942delinsTGAGAGCTCTGGTAG
XR_001740007.1:n.5928_5942delinsTGAGAGCTCTGGTAG
XR_001740008.1:n.5928_5942delinsTGAGAGCTCTGGTAG
XR_001740009.1:n.5928_5942delinsTGAGAGCTCTGGTAG
NM_000094.4:c.5892_5906delinsTGAGAGCTCTGGTAG MANE Select	NP_000085.1:p.Asp1964=