Canonical Allele Identifier: CA1363080173
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48566282T= , CM000665.2:g.48566282T= GRCh38
NC_000003.11:g.48603715T= , CM000665.1:g.48603715T= GRCh37
NC_000003.10:g.48578719T= NCBI36
NG_007065.1:g.33971A= , LRG_286:g.33971A=

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.8392A= MANE Select ENSP00000506558.1:p.Met2798=
ENST00000328333.12:c.8392A= ENSP00000332371.8:p.Met2798=
ENST00000487017.5:n.5031A=
NM_000094.3:c.8392A= , LRG_286t1:c.8392A= NP_000085.1:p.Met2798=
XM_011533336.1:c.8419A= XP_011531638.1:p.Met2807=
XM_011533337.1:c.8392A= XP_011531639.1:p.Met2798=
XM_011533338.1:c.8359A= XP_011531640.1:p.Met2787=
XR_940369.1:n.8455A=
XR_940370.1:n.8455A=
XR_940371.1:n.8455A=
XM_017005688.1:c.8332A= XP_016861177.1:p.Met2778=
XR_001740003.1:n.8428A=
XR_001740004.1:n.8428A=
XR_001740005.1:n.8428A=
NM_000094.4:c.8392A= MANE Select NP_000085.1:p.Met2798=