Canonical Allele Identifier: CA1363080171
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48566281A= , CM000665.2:g.48566281A= GRCh38
NC_000003.11:g.48603714A= , CM000665.1:g.48603714A= GRCh37
NC_000003.10:g.48578718A= NCBI36
NG_007065.1:g.33972T= , LRG_286:g.33972T=

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.8393T= MANE Select ENSP00000506558.1:p.Met2798=
ENST00000328333.12:c.8393T= ENSP00000332371.8:p.Met2798=
ENST00000487017.5:n.5032T=
NM_000094.3:c.8393T= , LRG_286t1:c.8393T= NP_000085.1:p.Met2798=
XM_011533336.1:c.8420T= XP_011531638.1:p.Met2807=
XM_011533337.1:c.8393T= XP_011531639.1:p.Met2798=
XM_011533338.1:c.8360T= XP_011531640.1:p.Met2787=
XR_940369.1:n.8456T=
XR_940370.1:n.8456T=
XR_940371.1:n.8456T=
XM_017005688.1:c.8333T= XP_016861177.1:p.Met2778=
XR_001740003.1:n.8429T=
XR_001740004.1:n.8429T=
XR_001740005.1:n.8429T=
NM_000094.4:c.8393T= MANE Select NP_000085.1:p.Met2798=