Canonical Allele Identifier: CA352642053

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48605593C>T (hg19) ; chr3:g.48568160C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568160C>T , CM000665.2:g.48568160C>T	GRCh38
NC_000003.11:g.48605593C>T , CM000665.1:g.48605593C>T	GRCh37
NC_000003.10:g.48580597C>T	NCBI36
NG_007065.1:g.32093G>A , LRG_286:g.32093G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7805G>A MANE Select	ENSP00000506558.1:p.Gly2602Glu
ENST00000328333.12:c.7805G>A	ENSP00000332371.8:p.Gly2602Glu
ENST00000459756.5:n.628G>A
ENST00000487017.5:n.4444G>A
NM_000094.3:c.7805G>A , LRG_286t1:c.7805G>A	NP_000085.1:p.Gly2602Glu
XM_011533336.1:c.7832G>A	XP_011531638.1:p.Gly2611Glu
XM_011533337.1:c.7805G>A	XP_011531639.1:p.Gly2602Glu
XM_011533338.1:c.7772G>A	XP_011531640.1:p.Gly2591Glu
XM_011533339.1:c.*37G>A	XP_011531641.1:n.*37G>A
XR_940369.1:n.7868G>A
XR_940370.1:n.7868G>A
XR_940371.1:n.7868G>A
XR_940372.1:n.7842G>A
XM_017005688.1:c.7745G>A	XP_016861177.1:p.Gly2582Glu
XM_017005689.1:c.*37G>A	XP_016861178.1:n.*37G>A
XR_001740003.1:n.7841G>A
XR_001740004.1:n.7841G>A
XR_001740005.1:n.7841G>A
XR_001740006.1:n.7815G>A
NM_000094.4:c.7805G>A MANE Select	NP_000085.1:p.Gly2602Glu