Canonical Allele Identifier: CA352645805

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48607598C>G (hg19) ; chr3:g.48570165C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48570165C>G , CM000665.2:g.48570165C>G	GRCh38
NC_000003.11:g.48607598C>G , CM000665.1:g.48607598C>G	GRCh37
NC_000003.10:g.48582602C>G	NCBI36
NG_007065.1:g.30088G>C , LRG_286:g.30088G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7454G>C MANE Select	ENSP00000506558.1:p.Arg2485Pro
ENST00000328333.12:c.7454G>C	ENSP00000332371.8:p.Arg2485Pro
ENST00000422991.1:c.449G>C	ENSP00000391608.1:p.Arg150Pro
ENST00000459756.5:n.277G>C
ENST00000467985.1:n.300G>C
ENST00000487017.5:n.4093G>C
NM_000094.3:c.7454G>C , LRG_286t1:c.7454G>C	NP_000085.1:p.Arg2485Pro
XM_011533336.1:c.7481G>C	XP_011531638.1:p.Arg2494Pro
XM_011533337.1:c.7454G>C	XP_011531639.1:p.Arg2485Pro
XM_011533338.1:c.7421G>C	XP_011531640.1:p.Arg2474Pro
XM_011533339.1:c.7481G>C	XP_011531641.1:p.Arg2494Pro
XM_011533340.1:c.*55G>C	XP_011531642.1:n.*55G>C
XM_011533341.1:c.*41G>C	XP_011531643.1:n.*41G>C
XM_011533342.1:c.*9G>C	XP_011531644.1:n.*9G>C
XR_940369.1:n.7517G>C
XR_940370.1:n.7517G>C
XR_940371.1:n.7517G>C
XR_940372.1:n.7491G>C
XM_017005688.1:c.7394G>C	XP_016861177.1:p.Arg2465Pro
XM_017005689.1:c.7454G>C	XP_016861178.1:p.Arg2485Pro
XM_017005690.1:c.*55G>C	XP_016861179.1:n.*55G>C
XM_017005691.1:c.*41G>C	XP_016861180.1:n.*41G>C
XM_017005692.1:c.*9G>C	XP_016861181.1:n.*9G>C
XR_001740003.1:n.7490G>C
XR_001740004.1:n.7490G>C
XR_001740005.1:n.7490G>C
XR_001740006.1:n.7464G>C
NM_000094.4:c.7454G>C MANE Select	NP_000085.1:p.Arg2485Pro