Canonical Allele Identifier: CA2377902

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48564940G>A , CM000665.2:g.48564940G>A	GRCh38
NC_000003.11:g.48602373G>A , CM000665.1:g.48602373G>A	GRCh37
NC_000003.10:g.48577377G>A	NCBI36
NG_007065.1:g.35313C>T , LRG_286:g.35313C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.8661C>T MANE Select	ENSP00000506558.1:p.Ala2887=
ENST00000328333.12:c.8661C>T	ENSP00000332371.8:p.Ala2887=
ENST00000465238.5:n.80C>T
ENST00000466591.1:n.272C>T
ENST00000470076.1:n.53C>T
ENST00000487017.5:n.5300C>T
NM_000094.3:c.8661C>T , LRG_286t1:c.8661C>T	NP_000085.1:p.Ala2887=
XM_011533336.1:c.8688C>T	XP_011531638.1:p.Ala2896=
XM_011533337.1:c.8661C>T	XP_011531639.1:p.Ala2887=
XM_011533338.1:c.8628C>T	XP_011531640.1:p.Ala2876=
XR_940369.1:n.8797C>T
XR_940370.1:n.8761C>T
XR_940371.1:n.8758C>T
XM_017005688.1:c.8601C>T	XP_016861177.1:p.Ala2867=
XR_001740003.1:n.8770C>T
XR_001740004.1:n.8734C>T
XR_001740005.1:n.8731C>T
NM_000094.4:c.8661C>T MANE Select	NP_000085.1:p.Ala2887=