Canonical Allele Identifier: CA2989547384

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48575437_48575438insTTGGGGAGAGGGGCCCCCCCGGGCCTTCCGGCCTTGCC , CM000665.2:g.48575437_48575438insTTGGGGAGAGGGGCCCCCCCGGGCCTTCCGGCCTTGCC	GRCh38
NC_000003.11:g.48612870_48612871insTTGGGGAGAGGGGCCCCCCCGGGCCTTCCGGCCTTGCC , CM000665.1:g.48612870_48612871insTTGGGGAGAGGGGCCCCCCCGGGCCTTCCGGCCTTGCC	GRCh37
NC_000003.10:g.48587874_48587875insTTGGGGAGAGGGGCCCCCCCGGGCCTTCCGGCCTTGCC	NCBI36
NG_007065.1:g.24817_24818insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG , LRG_286:g.24817_24818insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.6083_6084insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG MANE Select	ENSP00000506558.1:p.Pro2029LysfsTer?
ENST00000328333.12:c.6083_6084insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	ENSP00000332371.8:p.Pro2029LysfsTer?
ENST00000487017.5:n.2000_2001insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
NM_000094.3:c.6083_6084insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG , LRG_286t1:c.6083_6084insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	NP_000085.1:p.Pro2029LysfsTer?
XM_011533336.1:c.6110_6111insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	XP_011531638.1:p.Pro2038LysfsTer?
XM_011533337.1:c.6083_6084insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	XP_011531639.1:p.Pro2029LysfsTer?
XM_011533338.1:c.6110_6111insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	XP_011531640.1:p.Pro2038LysfsTer?
XM_011533339.1:c.6110_6111insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	XP_011531641.1:p.Pro2038LysfsTer?
XM_011533340.1:c.6110_6111insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	XP_011531642.1:p.Pro2038LysfsTer?
XM_011533341.1:c.6110_6111insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	XP_011531643.1:p.Pro2038LysfsTer?
XM_011533342.1:c.6110_6111insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	XP_011531644.1:p.Pro2038LysfsTer?
XR_940369.1:n.6146_6147insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XR_940370.1:n.6146_6147insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XR_940371.1:n.6146_6147insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XR_940372.1:n.6146_6147insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XR_940373.1:n.6146_6147insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XR_940374.1:n.6146_6147insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XR_940375.1:n.6146_6147insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XM_017005688.1:c.6083_6084insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	XP_016861177.1:p.Pro2029LysfsTer?
XM_017005689.1:c.6083_6084insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	XP_016861178.1:p.Pro2029LysfsTer?
XM_017005690.1:c.6083_6084insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	XP_016861179.1:p.Pro2029LysfsTer?
XM_017005691.1:c.6083_6084insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	XP_016861180.1:p.Pro2029LysfsTer?
XM_017005692.1:c.6083_6084insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG	XP_016861181.1:p.Pro2029LysfsTer?
XR_001740003.1:n.6119_6120insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XR_001740004.1:n.6119_6120insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XR_001740005.1:n.6119_6120insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XR_001740006.1:n.6119_6120insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XR_001740007.1:n.6119_6120insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XR_001740008.1:n.6119_6120insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
XR_001740009.1:n.6119_6120insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG
NM_000094.4:c.6083_6084insCAAGGCCGGAAGGCCCGGGGGGGCCCCTCTCCCCAAGG MANE Select	NP_000085.1:p.Pro2029LysfsTer?