Canonical Allele Identifier: CA2756157881

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48582417_48582418insAAACACACCCAACA , CM000665.2:g.48582417_48582418insAAACACACCCAACA	GRCh38
NC_000003.11:g.48619850_48619851insAAACACACCCAACA , CM000665.1:g.48619850_48619851insAAACACACCCAACA	GRCh37
NC_000003.10:g.48594854_48594855insAAACACACCCAACA	NCBI36
NG_007065.1:g.17835_17836insTGTTGGGTGTGTTT , LRG_286:g.17835_17836insTGTTGGGTGTGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.4600-60_4600-59insTGTTGGGTGTGTTT MANE Select	ENSP00000506558.1:n.4600-60_4600-59insTGTTGGGTGTGTTT
ENST00000328333.12:c.4600-60_4600-59insTGTTGGGTGTGTTT	ENSP00000332371.8:n.4600-60_4600-59insTGTTGGGTGTGTTT
ENST00000487017.5:n.517-60_517-59insTGTTGGGTGTGTTT
NM_000094.3:c.4600-60_4600-59insTGTTGGGTGTGTTT , LRG_286t1:c.4600-60_4600-59insTGTTGGGTGTGTTT	NP_000085.1:n.4600-60_4600-59insTGTTGGGTGTGTTT
XM_011533336.1:c.4627-60_4627-59insTGTTGGGTGTGTTT	XP_011531638.1:n.4627-60_4627-59insTGTTGGGTGTGTTT
XM_011533337.1:c.4600-60_4600-59insTGTTGGGTGTGTTT	XP_011531639.1:n.4600-60_4600-59insTGTTGGGTGTGTTT
XM_011533338.1:c.4627-60_4627-59insTGTTGGGTGTGTTT	XP_011531640.1:n.4627-60_4627-59insTGTTGGGTGTGTTT
XM_011533339.1:c.4627-60_4627-59insTGTTGGGTGTGTTT	XP_011531641.1:n.4627-60_4627-59insTGTTGGGTGTGTTT
XM_011533340.1:c.4627-60_4627-59insTGTTGGGTGTGTTT	XP_011531642.1:n.4627-60_4627-59insTGTTGGGTGTGTTT
XM_011533341.1:c.4627-60_4627-59insTGTTGGGTGTGTTT	XP_011531643.1:n.4627-60_4627-59insTGTTGGGTGTGTTT
XM_011533342.1:c.4627-60_4627-59insTGTTGGGTGTGTTT	XP_011531644.1:n.4627-60_4627-59insTGTTGGGTGTGTTT
XR_940369.1:n.4663-60_4663-59insTGTTGGGTGTGTTT
XR_940370.1:n.4663-60_4663-59insTGTTGGGTGTGTTT
XR_940371.1:n.4663-60_4663-59insTGTTGGGTGTGTTT
XR_940372.1:n.4663-60_4663-59insTGTTGGGTGTGTTT
XR_940373.1:n.4663-60_4663-59insTGTTGGGTGTGTTT
XR_940374.1:n.4663-60_4663-59insTGTTGGGTGTGTTT
XR_940375.1:n.4663-60_4663-59insTGTTGGGTGTGTTT
XM_017005688.1:c.4600-60_4600-59insTGTTGGGTGTGTTT	XP_016861177.1:n.4600-60_4600-59insTGTTGGGTGTGTTT
XM_017005689.1:c.4600-60_4600-59insTGTTGGGTGTGTTT	XP_016861178.1:n.4600-60_4600-59insTGTTGGGTGTGTTT
XM_017005690.1:c.4600-60_4600-59insTGTTGGGTGTGTTT	XP_016861179.1:n.4600-60_4600-59insTGTTGGGTGTGTTT
XM_017005691.1:c.4600-60_4600-59insTGTTGGGTGTGTTT	XP_016861180.1:n.4600-60_4600-59insTGTTGGGTGTGTTT
XM_017005692.1:c.4600-60_4600-59insTGTTGGGTGTGTTT	XP_016861181.1:n.4600-60_4600-59insTGTTGGGTGTGTTT
XR_001740003.1:n.4636-60_4636-59insTGTTGGGTGTGTTT
XR_001740004.1:n.4636-60_4636-59insTGTTGGGTGTGTTT
XR_001740005.1:n.4636-60_4636-59insTGTTGGGTGTGTTT
XR_001740006.1:n.4636-60_4636-59insTGTTGGGTGTGTTT
XR_001740007.1:n.4636-60_4636-59insTGTTGGGTGTGTTT
XR_001740008.1:n.4636-60_4636-59insTGTTGGGTGTGTTT
XR_001740009.1:n.4636-60_4636-59insTGTTGGGTGTGTTT
NM_000094.4:c.4600-60_4600-59insTGTTGGGTGTGTTT MANE Select	NP_000085.1:n.4600-60_4600-59insTGTTGGGTGTGTTT