Canonical Allele Identifier: CA433533338

Gene: COL7A1

Linked Data

• ClinVar Variation Id: 2772897
• ClinVar RCV Id: RCV003576910
• gnomAD v4: 3-48568811-T-G
• MyVariant Identifiers: chr3:g.48606244T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568811T>G , CM000665.2:g.48568811T>G	GRCh38
NC_000003.11:g.48606244T>G , CM000665.1:g.48606244T>G	GRCh37
NC_000003.10:g.48581248T>G	NCBI36
NG_007065.1:g.31442A>C , LRG_286:g.31442A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7731A>C MANE Select	ENSP00000506558.1:p.Pro2577=
ENST00000328333.12:c.7731A>C	ENSP00000332371.8:p.Pro2577=
ENST00000459756.5:n.554A>C
ENST00000467985.1:n.577A>C
ENST00000487017.5:n.4370A>C
NM_000094.3:c.7731A>C , LRG_286t1:c.7731A>C	NP_000085.1:p.Pro2577=
XM_011533336.1:c.7758A>C	XP_011531638.1:p.Pro2586=
XM_011533337.1:c.7731A>C	XP_011531639.1:p.Pro2577=
XM_011533338.1:c.7698A>C	XP_011531640.1:p.Pro2566=
XM_011533339.1:c.7758A>C	XP_011531641.1:p.Pro2586=
XR_940369.1:n.7794A>C
XR_940370.1:n.7794A>C
XR_940371.1:n.7794A>C
XR_940372.1:n.7768A>C
XM_017005688.1:c.7671A>C	XP_016861177.1:p.Pro2557=
XM_017005689.1:c.7731A>C	XP_016861178.1:p.Pro2577=
XR_001740003.1:n.7767A>C
XR_001740004.1:n.7767A>C
XR_001740005.1:n.7767A>C
XR_001740006.1:n.7741A>C
NM_000094.4:c.7731A>C MANE Select	NP_000085.1:p.Pro2577=