Canonical Allele Identifier: CA2665620099

Gene: COL7A1

Linked Data

• gnomAD v4: 3-48568767-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568767C>G , CM000665.2:g.48568767C>G	GRCh38
NC_000003.11:g.48606200C>G , CM000665.1:g.48606200C>G	GRCh37
NC_000003.10:g.48581204C>G	NCBI36
NG_007065.1:g.31486G>C , LRG_286:g.31486G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7758+17G>C MANE Select	ENSP00000506558.1:n.7758+17G>C
ENST00000328333.12:c.7758+17G>C	ENSP00000332371.8:n.7758+17G>C
ENST00000459756.5:n.581+17G>C
ENST00000467985.1:n.604+17G>C
ENST00000487017.5:n.4397+17G>C
NM_000094.3:c.7758+17G>C , LRG_286t1:c.7758+17G>C	NP_000085.1:n.7758+17G>C
XM_011533336.1:c.7785+17G>C	XP_011531638.1:n.7785+17G>C
XM_011533337.1:c.7758+17G>C	XP_011531639.1:n.7758+17G>C
XM_011533338.1:c.7725+17G>C	XP_011531640.1:n.7725+17G>C
XM_011533339.1:c.7785+17G>C	XP_011531641.1:n.7785+17G>C
XR_940369.1:n.7821+17G>C
XR_940370.1:n.7821+17G>C
XR_940371.1:n.7821+17G>C
XR_940372.1:n.7795+17G>C
XM_017005688.1:c.7698+17G>C	XP_016861177.1:n.7698+17G>C
XM_017005689.1:c.7758+17G>C	XP_016861178.1:n.7758+17G>C
XR_001740003.1:n.7794+17G>C
XR_001740004.1:n.7794+17G>C
XR_001740005.1:n.7794+17G>C
XR_001740006.1:n.7768+17G>C
NM_000094.4:c.7758+17G>C MANE Select	NP_000085.1:n.7758+17G>C