Canonical Allele Identifier: CA352645673
Gene: COL7A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48570147G>C , CM000665.2:g.48570147G>C GRCh38
NC_000003.11:g.48607580G>C , CM000665.1:g.48607580G>C GRCh37
NC_000003.10:g.48582584G>C NCBI36
NG_007065.1:g.30106C>G , LRG_286:g.30106C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.7472C>G MANE Select ENSP00000506558.1:p.Pro2491Arg
ENST00000328333.12:c.7472C>G ENSP00000332371.8:p.Pro2491Arg
ENST00000422991.1:c.467C>G ENSP00000391608.1:p.Pro156Arg
ENST00000459756.5:n.295C>G
ENST00000467985.1:n.318C>G
ENST00000487017.5:n.4111C>G
NM_000094.3:c.7472C>G , LRG_286t1:c.7472C>G NP_000085.1:p.Pro2491Arg
XM_011533336.1:c.7499C>G XP_011531638.1:p.Pro2500Arg
XM_011533337.1:c.7472C>G XP_011531639.1:p.Pro2491Arg
XM_011533338.1:c.7439C>G XP_011531640.1:p.Pro2480Arg
XM_011533339.1:c.7499C>G XP_011531641.1:p.Pro2500Arg
XM_011533342.1:c.*27C>G XP_011531644.1:n.*27C>G
XR_940369.1:n.7535C>G
XR_940370.1:n.7535C>G
XR_940371.1:n.7535C>G
XR_940372.1:n.7509C>G
XM_017005688.1:c.7412C>G XP_016861177.1:p.Pro2471Arg
XM_017005689.1:c.7472C>G XP_016861178.1:p.Pro2491Arg
XM_017005692.1:c.*27C>G XP_016861181.1:n.*27C>G
XR_001740003.1:n.7508C>G
XR_001740004.1:n.7508C>G
XR_001740005.1:n.7508C>G
XR_001740006.1:n.7482C>G
NM_000094.4:c.7472C>G MANE Select NP_000085.1:p.Pro2491Arg