Canonical Allele Identifier: CA2665614363

Gene: COL7A1

Linked Data

• gnomAD v4: 3-48572643-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48572643G>C , CM000665.2:g.48572643G>C	GRCh38
NC_000003.11:g.48610076G>C , CM000665.1:g.48610076G>C	GRCh37
NC_000003.10:g.48585080G>C	NCBI36
NG_007065.1:g.27610C>G , LRG_286:g.27610C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.6900+28C>G MANE Select	ENSP00000506558.1:n.6900+28C>G
ENST00000328333.12:c.6900+28C>G	ENSP00000332371.8:n.6900+28C>G
ENST00000487017.5:n.2817+28C>G
NM_000094.3:c.6900+28C>G , LRG_286t1:c.6900+28C>G	NP_000085.1:n.6900+28C>G
XM_011533336.1:c.6927+28C>G	XP_011531638.1:n.6927+28C>G
XM_011533337.1:c.6900+28C>G	XP_011531639.1:n.6900+28C>G
XM_011533338.1:c.6927+28C>G	XP_011531640.1:n.6927+28C>G
XM_011533339.1:c.6927+28C>G	XP_011531641.1:n.6927+28C>G
XM_011533340.1:c.6927+28C>G	XP_011531642.1:n.6927+28C>G
XM_011533341.1:c.6927+28C>G	XP_011531643.1:n.6927+28C>G
XM_011533342.1:c.6927+28C>G	XP_011531644.1:n.6927+28C>G
XR_940369.1:n.6963+28C>G
XR_940370.1:n.6963+28C>G
XR_940371.1:n.6963+28C>G
XR_940372.1:n.6963+28C>G
XR_940373.1:n.6963+28C>G
XR_940374.1:n.6973+28C>G
XM_017005688.1:c.6900+28C>G	XP_016861177.1:n.6900+28C>G
XM_017005689.1:c.6900+28C>G	XP_016861178.1:n.6900+28C>G
XM_017005690.1:c.6900+28C>G	XP_016861179.1:n.6900+28C>G
XM_017005691.1:c.6900+28C>G	XP_016861180.1:n.6900+28C>G
XM_017005692.1:c.6900+28C>G	XP_016861181.1:n.6900+28C>G
XR_001740003.1:n.6936+28C>G
XR_001740004.1:n.6936+28C>G
XR_001740005.1:n.6936+28C>G
XR_001740006.1:n.6936+28C>G
XR_001740007.1:n.6936+28C>G
XR_001740008.1:n.6946+28C>G
NM_000094.4:c.6900+28C>G MANE Select	NP_000085.1:n.6900+28C>G