Canonical Allele Identifier: CA2377977
Community Standard Title: NM_000094.4(COL7A1):c.8504G>A (p.Arg2835His)
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48565433C>T , CM000665.2:g.48565433C>T GRCh38
NC_000003.11:g.48602866C>T , CM000665.1:g.48602866C>T GRCh37
NC_000003.10:g.48577870C>T NCBI36
NG_007065.1:g.34820G>A , LRG_286:g.34820G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000094.4:c.8504G>A MANE Select NP_000085.1:p.Arg2835His
ENST00000681320.1:c.8504G>A MANE Select ENSP00000506558.1:p.Arg2835His
NM_000094.3:c.8504G>A , LRG_286t1:c.8504G>A NP_000085.1:p.Arg2835His
ENST00000328333.12:c.8504G>A ENSP00000332371.8:p.Arg2835His
ENST00000487017.5:n.5143G>A
XM_011533336.1:c.8531G>A XP_011531638.1:p.Arg2844His
XM_011533337.1:c.8504G>A XP_011531639.1:p.Arg2835His
XM_011533338.1:c.8471G>A XP_011531640.1:p.Arg2824His
XM_017005688.1:c.8444G>A XP_016861177.1:p.Arg2815His
XR_001740003.1:n.8540G>A
XR_001740004.1:n.8540G>A
XR_001740005.1:n.8540G>A
XR_940369.1:n.8567G>A
XR_940370.1:n.8567G>A
XR_940371.1:n.8567G>A