Canonical Allele Identifier: CA2379130

Gene: COL7A1

Linked Data

• ClinVar Variation Id: 1481757
• ClinVar RCV Id: RCV002000622
• dbSNP Id: rs139920321
• ExAC: 3:48612511 G / A
• gnomAD v2: 3-48612511-G-A
• gnomAD v3: 3-48575078-G-A
• gnomAD v4: 3-48575078-G-A
• MyVariant Identifiers: chr3:g.48612511G>A (hg19) ; chr3:g.48575078G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48575078G>A , CM000665.2:g.48575078G>A	GRCh38
NC_000003.11:g.48612511G>A , CM000665.1:g.48612511G>A	GRCh37
NC_000003.10:g.48587515G>A	NCBI36
NG_007065.1:g.25175C>T , LRG_286:g.25175C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.6265C>T MANE Select	ENSP00000506558.1:p.Pro2089Ser
ENST00000328333.12:c.6265C>T	ENSP00000332371.8:p.Pro2089Ser
ENST00000487017.5:n.2182C>T
NM_000094.3:c.6265C>T , LRG_286t1:c.6265C>T	NP_000085.1:p.Pro2089Ser
XM_011533336.1:c.6292C>T	XP_011531638.1:p.Pro2098Ser
XM_011533337.1:c.6265C>T	XP_011531639.1:p.Pro2089Ser
XM_011533338.1:c.6292C>T	XP_011531640.1:p.Pro2098Ser
XM_011533339.1:c.6292C>T	XP_011531641.1:p.Pro2098Ser
XM_011533340.1:c.6292C>T	XP_011531642.1:p.Pro2098Ser
XM_011533341.1:c.6292C>T	XP_011531643.1:p.Pro2098Ser
XM_011533342.1:c.6292C>T	XP_011531644.1:p.Pro2098Ser
XR_940369.1:n.6328C>T
XR_940370.1:n.6328C>T
XR_940371.1:n.6328C>T
XR_940372.1:n.6328C>T
XR_940373.1:n.6328C>T
XR_940374.1:n.6328C>T
XR_940375.1:n.6266C>T
XM_017005688.1:c.6265C>T	XP_016861177.1:p.Pro2089Ser
XM_017005689.1:c.6265C>T	XP_016861178.1:p.Pro2089Ser
XM_017005690.1:c.6265C>T	XP_016861179.1:p.Pro2089Ser
XM_017005691.1:c.6265C>T	XP_016861180.1:p.Pro2089Ser
XM_017005692.1:c.6265C>T	XP_016861181.1:p.Pro2089Ser
XR_001740003.1:n.6301C>T
XR_001740004.1:n.6301C>T
XR_001740005.1:n.6301C>T
XR_001740006.1:n.6301C>T
XR_001740007.1:n.6301C>T
XR_001740008.1:n.6301C>T
XR_001740009.1:n.6239C>T
NM_000094.4:c.6265C>T MANE Select	NP_000085.1:p.Pro2089Ser