Canonical Allele Identifier: CA352632458

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48564794C>A , CM000665.2:g.48564794C>A	GRCh38
NC_000003.11:g.48602227C>A , CM000665.1:g.48602227C>A	GRCh37
NC_000003.10:g.48577231C>A	NCBI36
NG_007065.1:g.35459G>T , LRG_286:g.35459G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.8807G>T MANE Select	ENSP00000506558.1:p.Ser2936Ile
ENST00000328333.12:c.8807G>T	ENSP00000332371.8:p.Ser2936Ile
ENST00000465238.5:n.226G>T
ENST00000466591.1:n.418G>T
ENST00000470076.1:n.199G>T
ENST00000487017.5:n.5446G>T
NM_000094.3:c.8807G>T , LRG_286t1:c.8807G>T	NP_000085.1:p.Ser2936Ile
XM_011533336.1:c.8834G>T	XP_011531638.1:p.Ser2945Ile
XM_011533337.1:c.8807G>T	XP_011531639.1:p.Ser2936Ile
XM_011533338.1:c.8774G>T	XP_011531640.1:p.Ser2925Ile
XR_940369.1:n.8943G>T
XR_940370.1:n.8907G>T
XR_940371.1:n.8904G>T
XM_017005688.1:c.8747G>T	XP_016861177.1:p.Ser2916Ile
XR_001740003.1:n.8916G>T
XR_001740004.1:n.8880G>T
XR_001740005.1:n.8877G>T
NM_000094.4:c.8807G>T MANE Select	NP_000085.1:p.Ser2936Ile