Canonical Allele Identifier: CA1363079282

Gene: COL7A1

Linked Data

• dbSNP Id: rs1575423920

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48570113A>C , CM000665.2:g.48570113A>C	GRCh38
NC_000003.11:g.48607546A>C , CM000665.1:g.48607546A>C	GRCh37
NC_000003.10:g.48582550A>C	NCBI36
NG_007065.1:g.30140T>G , LRG_286:g.30140T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7485+21T>G MANE Select	ENSP00000506558.1:n.7485+21T>G
ENST00000328333.12:c.7485+21T>G	ENSP00000332371.8:n.7485+21T>G
ENST00000422991.1:c.480+21T>G	ENSP00000391608.1:n.480+21T>G
ENST00000459756.5:n.308+21T>G
ENST00000467985.1:n.331+21T>G
ENST00000487017.5:n.4124+21T>G
NM_000094.3:c.7485+21T>G , LRG_286t1:c.7485+21T>G	NP_000085.1:n.7485+21T>G
XM_011533336.1:c.7512+21T>G	XP_011531638.1:n.7512+21T>G
XM_011533337.1:c.7485+21T>G	XP_011531639.1:n.7485+21T>G
XM_011533338.1:c.7452+21T>G	XP_011531640.1:n.7452+21T>G
XM_011533339.1:c.7512+21T>G	XP_011531641.1:n.7512+21T>G
XM_011533342.1:c.*40+21T>G	XP_011531644.1:n.*40+21T>G
XR_940369.1:n.7548+21T>G
XR_940370.1:n.7548+21T>G
XR_940371.1:n.7548+21T>G
XR_940372.1:n.7522+21T>G
XM_017005688.1:c.7425+21T>G	XP_016861177.1:n.7425+21T>G
XM_017005689.1:c.7485+21T>G	XP_016861178.1:n.7485+21T>G
XM_017005692.1:c.*40+21T>G	XP_016861181.1:n.*40+21T>G
XR_001740003.1:n.7521+21T>G
XR_001740004.1:n.7521+21T>G
XR_001740005.1:n.7521+21T>G
XR_001740006.1:n.7495+21T>G
NM_000094.4:c.7485+21T>G MANE Select	NP_000085.1:n.7485+21T>G