Canonical Allele Identifier: CA433533240

Gene: COL7A1

Linked Data

• ClinVar Variation Id: 1912886
• ClinVar RCV Id: RCV002601128
• dbSNP Id: rs1175960041
• gnomAD v3: 3-48568526-A-G
• gnomAD v4: 3-48568526-A-G
• MyVariant Identifiers: chr3:g.48605959A>G (hg19) ; chr3:g.48568526A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568526A>G , CM000665.2:g.48568526A>G	GRCh38
NC_000003.11:g.48605959A>G , CM000665.1:g.48605959A>G	GRCh37
NC_000003.10:g.48580963A>G	NCBI36
NG_007065.1:g.31727T>C , LRG_286:g.31727T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7767T>C MANE Select	ENSP00000506558.1:p.Pro2589=
ENST00000328333.12:c.7767T>C	ENSP00000332371.8:p.Pro2589=
ENST00000459756.5:n.590T>C
ENST00000467985.1:n.613T>C
ENST00000487017.5:n.4406T>C
NM_000094.3:c.7767T>C , LRG_286t1:c.7767T>C	NP_000085.1:p.Pro2589=
XM_011533336.1:c.7794T>C	XP_011531638.1:p.Pro2598=
XM_011533337.1:c.7767T>C	XP_011531639.1:p.Pro2589=
XM_011533338.1:c.7734T>C	XP_011531640.1:p.Pro2578=
XM_011533339.1:c.7794T>C	XP_011531641.1:p.Pro2598=
XR_940369.1:n.7830T>C
XR_940370.1:n.7830T>C
XR_940371.1:n.7830T>C
XR_940372.1:n.7804T>C
XM_017005688.1:c.7707T>C	XP_016861177.1:p.Pro2569=
XM_017005689.1:c.7767T>C	XP_016861178.1:p.Pro2589=
XR_001740003.1:n.7803T>C
XR_001740004.1:n.7803T>C
XR_001740005.1:n.7803T>C
XR_001740006.1:n.7777T>C
NM_000094.4:c.7767T>C MANE Select	NP_000085.1:p.Pro2589=