Canonical Allele Identifier: CA2377879

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48564821C>T , CM000665.2:g.48564821C>T	GRCh38
NC_000003.11:g.48602254C>T , CM000665.1:g.48602254C>T	GRCh37
NC_000003.10:g.48577258C>T	NCBI36
NG_007065.1:g.35432G>A , LRG_286:g.35432G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.8780G>A MANE Select	ENSP00000506558.1:p.Arg2927His
ENST00000328333.12:c.8780G>A	ENSP00000332371.8:p.Arg2927His
ENST00000465238.5:n.199G>A
ENST00000466591.1:n.391G>A
ENST00000470076.1:n.172G>A
ENST00000487017.5:n.5419G>A
NM_000094.3:c.8780G>A , LRG_286t1:c.8780G>A	NP_000085.1:p.Arg2927His
XM_011533336.1:c.8807G>A	XP_011531638.1:p.Arg2936His
XM_011533337.1:c.8780G>A	XP_011531639.1:p.Arg2927His
XM_011533338.1:c.8747G>A	XP_011531640.1:p.Arg2916His
XR_940369.1:n.8916G>A
XR_940370.1:n.8880G>A
XR_940371.1:n.8877G>A
XM_017005688.1:c.8720G>A	XP_016861177.1:p.Arg2907His
XR_001740003.1:n.8889G>A
XR_001740004.1:n.8853G>A
XR_001740005.1:n.8850G>A
NM_000094.4:c.8780G>A MANE Select	NP_000085.1:p.Arg2927His