Canonical Allele Identifier: CA2379404

Gene: COL7A1

Linked Data

• ClinVar Variation Id: 345833
• ClinVar RCV Id: RCV000303583 ; RCV002057884
• dbSNP Id: rs200309694
• ExAC: 3:48614219 G / A
• gnomAD v2: 3-48614219-G-A
• gnomAD v3: 3-48576786-G-A
• gnomAD v4: 3-48576786-G-A
• MyVariant Identifiers: chr3:g.48614219G>A (hg19) ; chr3:g.48576786G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48576786G>A , CM000665.2:g.48576786G>A	GRCh38
NC_000003.11:g.48614219G>A , CM000665.1:g.48614219G>A	GRCh37
NC_000003.10:g.48589223G>A	NCBI36
NG_007065.1:g.23467C>T , LRG_286:g.23467C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.5605-15C>T MANE Select	ENSP00000506558.1:n.5605-15C>T
ENST00000328333.12:c.5605-15C>T	ENSP00000332371.8:n.5605-15C>T
ENST00000487017.5:n.1522-15C>T
NM_000094.3:c.5605-15C>T , LRG_286t1:c.5605-15C>T	NP_000085.1:n.5605-15C>T
XM_011533336.1:c.5632-15C>T	XP_011531638.1:n.5632-15C>T
XM_011533337.1:c.5605-15C>T	XP_011531639.1:n.5605-15C>T
XM_011533338.1:c.5632-15C>T	XP_011531640.1:n.5632-15C>T
XM_011533339.1:c.5632-15C>T	XP_011531641.1:n.5632-15C>T
XM_011533340.1:c.5632-15C>T	XP_011531642.1:n.5632-15C>T
XM_011533341.1:c.5632-15C>T	XP_011531643.1:n.5632-15C>T
XM_011533342.1:c.5632-15C>T	XP_011531644.1:n.5632-15C>T
XR_940369.1:n.5668-15C>T
XR_940370.1:n.5668-15C>T
XR_940371.1:n.5668-15C>T
XR_940372.1:n.5668-15C>T
XR_940373.1:n.5668-15C>T
XR_940374.1:n.5668-15C>T
XR_940375.1:n.5668-15C>T
XM_017005688.1:c.5605-15C>T	XP_016861177.1:n.5605-15C>T
XM_017005689.1:c.5605-15C>T	XP_016861178.1:n.5605-15C>T
XM_017005690.1:c.5605-15C>T	XP_016861179.1:n.5605-15C>T
XM_017005691.1:c.5605-15C>T	XP_016861180.1:n.5605-15C>T
XM_017005692.1:c.5605-15C>T	XP_016861181.1:n.5605-15C>T
XR_001740003.1:n.5641-15C>T
XR_001740004.1:n.5641-15C>T
XR_001740005.1:n.5641-15C>T
XR_001740006.1:n.5641-15C>T
XR_001740007.1:n.5641-15C>T
XR_001740008.1:n.5641-15C>T
XR_001740009.1:n.5641-15C>T
NM_000094.4:c.5605-15C>T MANE Select	NP_000085.1:n.5605-15C>T