Canonical Allele Identifier: CA2499216842

Gene: COL7A1

Linked Data

• ClinVar Variation Id: 1108774
• ClinVar RCV Id: RCV001434353
• dbSNP Id: rs2107645388

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48570268T>A , CM000665.2:g.48570268T>A	GRCh38
NC_000003.11:g.48607701T>A , CM000665.1:g.48607701T>A	GRCh37
NC_000003.10:g.48582705T>A	NCBI36
NG_007065.1:g.29985A>T , LRG_286:g.29985A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7440+7A>T MANE Select	ENSP00000506558.1:n.7440+7A>T
ENST00000328333.12:c.7440+7A>T	ENSP00000332371.8:n.7440+7A>T
ENST00000422991.1:c.435+7A>T	ENSP00000391608.1:n.435+7A>T
ENST00000459756.5:n.174A>T
ENST00000467985.1:n.197A>T
ENST00000487017.5:n.4079+7A>T
NM_000094.3:c.7440+7A>T , LRG_286t1:c.7440+7A>T	NP_000085.1:n.7440+7A>T
XM_011533336.1:c.7467+7A>T	XP_011531638.1:n.7467+7A>T
XM_011533337.1:c.7440+7A>T	XP_011531639.1:n.7440+7A>T
XM_011533338.1:c.7408-90A>T	XP_011531640.1:n.7408-90A>T
XM_011533339.1:c.7467+7A>T	XP_011531641.1:n.7467+7A>T
XM_011533340.1:c.7408-16A>T	XP_011531642.1:n.7408-16A>T
XM_011533341.1:c.7382-16A>T	XP_011531643.1:n.7382-16A>T
XM_011533342.1:c.7382-90A>T	XP_011531644.1:n.7382-90A>T
XR_940369.1:n.7503+7A>T
XR_940370.1:n.7503+7A>T
XR_940371.1:n.7503+7A>T
XR_940372.1:n.7477+7A>T
XM_017005688.1:c.7381-90A>T	XP_016861177.1:n.7381-90A>T
XM_017005689.1:c.7440+7A>T	XP_016861178.1:n.7440+7A>T
XM_017005690.1:c.7381-16A>T	XP_016861179.1:n.7381-16A>T
XM_017005691.1:c.7355-16A>T	XP_016861180.1:n.7355-16A>T
XM_017005692.1:c.7355-90A>T	XP_016861181.1:n.7355-90A>T
XR_001740003.1:n.7476+7A>T
XR_001740004.1:n.7476+7A>T
XR_001740005.1:n.7476+7A>T
XR_001740006.1:n.7450+7A>T
NM_000094.4:c.7440+7A>T MANE Select	NP_000085.1:n.7440+7A>T