Canonical Allele Identifier: CA2665615727

Gene: COL7A1

Linked Data

• gnomAD v4: 3-48565545-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48565545C>A , CM000665.2:g.48565545C>A	GRCh38
NC_000003.11:g.48602978C>A , CM000665.1:g.48602978C>A	GRCh37
NC_000003.10:g.48577982C>A	NCBI36
NG_007065.1:g.34708G>T , LRG_286:g.34708G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.8441-49G>T MANE Select	ENSP00000506558.1:n.8441-49G>T
ENST00000328333.12:c.8441-49G>T	ENSP00000332371.8:n.8441-49G>T
ENST00000487017.5:n.5080-49G>T
NM_000094.3:c.8441-49G>T , LRG_286t1:c.8441-49G>T	NP_000085.1:n.8441-49G>T
XM_011533336.1:c.8468-49G>T	XP_011531638.1:n.8468-49G>T
XM_011533337.1:c.8441-49G>T	XP_011531639.1:n.8441-49G>T
XM_011533338.1:c.8408-49G>T	XP_011531640.1:n.8408-49G>T
XR_940369.1:n.8504-49G>T
XR_940370.1:n.8504-49G>T
XR_940371.1:n.8504-49G>T
XM_017005688.1:c.8381-49G>T	XP_016861177.1:n.8381-49G>T
XR_001740003.1:n.8477-49G>T
XR_001740004.1:n.8477-49G>T
XR_001740005.1:n.8477-49G>T
NM_000094.4:c.8441-49G>T MANE Select	NP_000085.1:n.8441-49G>T