Canonical Allele Identifier: CA433533864

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48607597G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48570164G>T , CM000665.2:g.48570164G>T	GRCh38
NC_000003.11:g.48607597G>T , CM000665.1:g.48607597G>T	GRCh37
NC_000003.10:g.48582601G>T	NCBI36
NG_007065.1:g.30089C>A , LRG_286:g.30089C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7455C>A MANE Select	ENSP00000506558.1:p.Arg2485=
ENST00000328333.12:c.7455C>A	ENSP00000332371.8:p.Arg2485=
ENST00000422991.1:c.450C>A	ENSP00000391608.1:p.Arg150=
ENST00000459756.5:n.278C>A
ENST00000467985.1:n.301C>A
ENST00000487017.5:n.4094C>A
NM_000094.3:c.7455C>A , LRG_286t1:c.7455C>A	NP_000085.1:p.Arg2485=
XM_011533336.1:c.7482C>A	XP_011531638.1:p.Arg2494=
XM_011533337.1:c.7455C>A	XP_011531639.1:p.Arg2485=
XM_011533338.1:c.7422C>A	XP_011531640.1:p.Arg2474=
XM_011533339.1:c.7482C>A	XP_011531641.1:p.Arg2494=
XM_011533340.1:c.*56C>A	XP_011531642.1:n.*56C>A
XM_011533341.1:c.*42C>A	XP_011531643.1:n.*42C>A
XM_011533342.1:c.*10C>A	XP_011531644.1:n.*10C>A
XR_940369.1:n.7518C>A
XR_940370.1:n.7518C>A
XR_940371.1:n.7518C>A
XR_940372.1:n.7492C>A
XM_017005688.1:c.7395C>A	XP_016861177.1:p.Arg2465=
XM_017005689.1:c.7455C>A	XP_016861178.1:p.Arg2485=
XM_017005690.1:c.*56C>A	XP_016861179.1:n.*56C>A
XM_017005691.1:c.*42C>A	XP_016861180.1:n.*42C>A
XM_017005692.1:c.*10C>A	XP_016861181.1:n.*10C>A
XR_001740003.1:n.7491C>A
XR_001740004.1:n.7491C>A
XR_001740005.1:n.7491C>A
XR_001740006.1:n.7465C>A
NM_000094.4:c.7455C>A MANE Select	NP_000085.1:p.Arg2485=