Canonical Allele Identifier: CA2665619852

Gene: COL7A1

Linked Data

• gnomAD v4: 3-48568542-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568542A>G , CM000665.2:g.48568542A>G	GRCh38
NC_000003.11:g.48605975A>G , CM000665.1:g.48605975A>G	GRCh37
NC_000003.10:g.48580979A>G	NCBI36
NG_007065.1:g.31711T>C , LRG_286:g.31711T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7759-8T>C MANE Select	ENSP00000506558.1:n.7759-8T>C
ENST00000328333.12:c.7759-8T>C	ENSP00000332371.8:n.7759-8T>C
ENST00000459756.5:n.582-8T>C
ENST00000467985.1:n.605-8T>C
ENST00000487017.5:n.4398-8T>C
NM_000094.3:c.7759-8T>C , LRG_286t1:c.7759-8T>C	NP_000085.1:n.7759-8T>C
XM_011533336.1:c.7786-8T>C	XP_011531638.1:n.7786-8T>C
XM_011533337.1:c.7759-8T>C	XP_011531639.1:n.7759-8T>C
XM_011533338.1:c.7726-8T>C	XP_011531640.1:n.7726-8T>C
XM_011533339.1:c.7786-8T>C	XP_011531641.1:n.7786-8T>C
XR_940369.1:n.7822-8T>C
XR_940370.1:n.7822-8T>C
XR_940371.1:n.7822-8T>C
XR_940372.1:n.7796-8T>C
XM_017005688.1:c.7699-8T>C	XP_016861177.1:n.7699-8T>C
XM_017005689.1:c.7759-8T>C	XP_016861178.1:n.7759-8T>C
XR_001740003.1:n.7795-8T>C
XR_001740004.1:n.7795-8T>C
XR_001740005.1:n.7795-8T>C
XR_001740006.1:n.7769-8T>C
NM_000094.4:c.7759-8T>C MANE Select	NP_000085.1:n.7759-8T>C