Canonical Allele Identifier: CA2377953

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48565246C>T , CM000665.2:g.48565246C>T	GRCh38
NC_000003.11:g.48602679C>T , CM000665.1:g.48602679C>T	GRCh37
NC_000003.10:g.48577683C>T	NCBI36
NG_007065.1:g.35007G>A , LRG_286:g.35007G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000094.4:c.8528-45G>A MANE Select	NP_000085.1:n.8528-45G>A
ENST00000681320.1:c.8528-45G>A MANE Select	ENSP00000506558.1:n.8528-45G>A
NM_000094.3:c.8528-45G>A , LRG_286t1:c.8528-45G>A	NP_000085.1:n.8528-45G>A
ENST00000328333.12:c.8528-45G>A	ENSP00000332371.8:n.8528-45G>A
ENST00000466591.1:n.94G>A
ENST00000487017.5:n.5167-45G>A
XM_011533336.1:c.8555-45G>A	XP_011531638.1:n.8555-45G>A
XM_011533337.1:c.8528-45G>A	XP_011531639.1:n.8528-45G>A
XM_011533338.1:c.8495-45G>A	XP_011531640.1:n.8495-45G>A
XM_017005688.1:c.8468-45G>A	XP_016861177.1:n.8468-45G>A
XR_001740003.1:n.8592G>A
XR_001740004.1:n.8564-8G>A
XR_001740005.1:n.8564-11G>A
XR_940369.1:n.8619G>A
XR_940370.1:n.8591-8G>A
XR_940371.1:n.8591-11G>A