Canonical Allele Identifier: CA352649756
Community Standard Title: NM_000094.4(COL7A1):c.7270C>T (p.Arg2424Trp)
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48570863G>A , CM000665.2:g.48570863G>A GRCh38
NC_000003.11:g.48608296G>A , CM000665.1:g.48608296G>A GRCh37
NC_000003.10:g.48583300G>A NCBI36
NG_007065.1:g.29390C>T , LRG_286:g.29390C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000094.4:c.7270C>T MANE Select NP_000085.1:p.Arg2424Trp
ENST00000681320.1:c.7270C>T MANE Select ENSP00000506558.1:p.Arg2424Trp
NM_000094.3:c.7270C>T , LRG_286t1:c.7270C>T NP_000085.1:p.Arg2424Trp
ENST00000328333.12:c.7270C>T ENSP00000332371.8:p.Arg2424Trp
ENST00000422991.1:c.265C>T ENSP00000391608.1:p.Arg89Trp
ENST00000467985.1:n.20C>T
ENST00000487017.5:n.3909C>T
XM_011533336.1:c.7297C>T XP_011531638.1:p.Arg2433Trp
XM_011533337.1:c.7270C>T XP_011531639.1:p.Arg2424Trp
XM_011533338.1:c.7297C>T XP_011531640.1:p.Arg2433Trp
XM_011533339.1:c.7297C>T XP_011531641.1:p.Arg2433Trp
XM_011533340.1:c.7297C>T XP_011531642.1:p.Arg2433Trp
XM_011533341.1:c.7273+24C>T XP_011531643.1:n.7273+24C>T
XM_011533342.1:c.7273+24C>T XP_011531644.1:n.7273+24C>T
XM_017005688.1:c.7270C>T XP_016861177.1:p.Arg2424Trp
XM_017005689.1:c.7270C>T XP_016861178.1:p.Arg2424Trp
XM_017005690.1:c.7270C>T XP_016861179.1:p.Arg2424Trp
XM_017005691.1:c.7246+24C>T XP_016861180.1:n.7246+24C>T
XM_017005692.1:c.7246+24C>T XP_016861181.1:n.7246+24C>T
XR_001740003.1:n.7306C>T
XR_001740004.1:n.7306C>T
XR_001740005.1:n.7306C>T
XR_001740006.1:n.7282+24C>T
XR_940369.1:n.7333C>T
XR_940370.1:n.7333C>T
XR_940371.1:n.7333C>T
XR_940372.1:n.7309+24C>T