Canonical Allele Identifier: CA352643362

Gene: COL7A1

Linked Data

• gnomAD v4: 3-48568849-T-G
• MyVariant Identifiers: chr3:g.48606282T>G (hg19) ; chr3:g.48568849T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568849T>G , CM000665.2:g.48568849T>G	GRCh38
NC_000003.11:g.48606282T>G , CM000665.1:g.48606282T>G	GRCh37
NC_000003.10:g.48581286T>G	NCBI36
NG_007065.1:g.31404A>C , LRG_286:g.31404A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7693A>C MANE Select	ENSP00000506558.1:p.Lys2565Gln
ENST00000328333.12:c.7693A>C	ENSP00000332371.8:p.Lys2565Gln
ENST00000459756.5:n.516A>C
ENST00000467985.1:n.539A>C
ENST00000487017.5:n.4332A>C
NM_000094.3:c.7693A>C , LRG_286t1:c.7693A>C	NP_000085.1:p.Lys2565Gln
XM_011533336.1:c.7720A>C	XP_011531638.1:p.Lys2574Gln
XM_011533337.1:c.7693A>C	XP_011531639.1:p.Lys2565Gln
XM_011533338.1:c.7660A>C	XP_011531640.1:p.Lys2554Gln
XM_011533339.1:c.7720A>C	XP_011531641.1:p.Lys2574Gln
XR_940369.1:n.7756A>C
XR_940370.1:n.7756A>C
XR_940371.1:n.7756A>C
XR_940372.1:n.7730A>C
XM_017005688.1:c.7633A>C	XP_016861177.1:p.Lys2545Gln
XM_017005689.1:c.7693A>C	XP_016861178.1:p.Lys2565Gln
XR_001740003.1:n.7729A>C
XR_001740004.1:n.7729A>C
XR_001740005.1:n.7729A>C
XR_001740006.1:n.7703A>C
NM_000094.4:c.7693A>C MANE Select	NP_000085.1:p.Lys2565Gln