Canonical Allele Identifier: CA433533949

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48607714G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48570281G>C , CM000665.2:g.48570281G>C	GRCh38
NC_000003.11:g.48607714G>C , CM000665.1:g.48607714G>C	GRCh37
NC_000003.10:g.48582718G>C	NCBI36
NG_007065.1:g.29972C>G , LRG_286:g.29972C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7434C>G MANE Select	ENSP00000506558.1:p.Gly2478=
ENST00000328333.12:c.7434C>G	ENSP00000332371.8:p.Gly2478=
ENST00000422991.1:c.429C>G	ENSP00000391608.1:p.Gly143=
ENST00000459756.5:n.161C>G
ENST00000467985.1:n.184C>G
ENST00000487017.5:n.4073C>G
NM_000094.3:c.7434C>G , LRG_286t1:c.7434C>G	NP_000085.1:p.Gly2478=
XM_011533336.1:c.7461C>G	XP_011531638.1:p.Gly2487=
XM_011533337.1:c.7434C>G	XP_011531639.1:p.Gly2478=
XM_011533338.1:c.7408-103C>G	XP_011531640.1:n.7408-103C>G
XM_011533339.1:c.7461C>G	XP_011531641.1:p.Gly2487=
XM_011533340.1:c.7408-29C>G	XP_011531642.1:n.7408-29C>G
XM_011533341.1:c.7382-29C>G	XP_011531643.1:n.7382-29C>G
XM_011533342.1:c.7382-103C>G	XP_011531644.1:n.7382-103C>G
XR_940369.1:n.7497C>G
XR_940370.1:n.7497C>G
XR_940371.1:n.7497C>G
XR_940372.1:n.7471C>G
XM_017005688.1:c.7381-103C>G	XP_016861177.1:n.7381-103C>G
XM_017005689.1:c.7434C>G	XP_016861178.1:p.Gly2478=
XM_017005690.1:c.7381-29C>G	XP_016861179.1:n.7381-29C>G
XM_017005691.1:c.7355-29C>G	XP_016861180.1:n.7355-29C>G
XM_017005692.1:c.7355-103C>G	XP_016861181.1:n.7355-103C>G
XR_001740003.1:n.7470C>G
XR_001740004.1:n.7470C>G
XR_001740005.1:n.7470C>G
XR_001740006.1:n.7444C>G
NM_000094.4:c.7434C>G MANE Select	NP_000085.1:p.Gly2478=