Canonical Allele Identifier: CA433533838

Gene: COL7A1

Linked Data

• ClinVar Variation Id: 1122499
• ClinVar RCV Id: RCV001453174
• dbSNP Id: rs1484220256
• MyVariant Identifiers: chr3:g.48607579G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48570146G>C , CM000665.2:g.48570146G>C	GRCh38
NC_000003.11:g.48607579G>C , CM000665.1:g.48607579G>C	GRCh37
NC_000003.10:g.48582583G>C	NCBI36
NG_007065.1:g.30107C>G , LRG_286:g.30107C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7473C>G MANE Select	ENSP00000506558.1:p.Pro2491=
ENST00000328333.12:c.7473C>G	ENSP00000332371.8:p.Pro2491=
ENST00000422991.1:c.468C>G	ENSP00000391608.1:p.Pro156=
ENST00000459756.5:n.296C>G
ENST00000467985.1:n.319C>G
ENST00000487017.5:n.4112C>G
NM_000094.3:c.7473C>G , LRG_286t1:c.7473C>G	NP_000085.1:p.Pro2491=
XM_011533336.1:c.7500C>G	XP_011531638.1:p.Pro2500=
XM_011533337.1:c.7473C>G	XP_011531639.1:p.Pro2491=
XM_011533338.1:c.7440C>G	XP_011531640.1:p.Pro2480=
XM_011533339.1:c.7500C>G	XP_011531641.1:p.Pro2500=
XM_011533342.1:c.*28C>G	XP_011531644.1:n.*28C>G
XR_940369.1:n.7536C>G
XR_940370.1:n.7536C>G
XR_940371.1:n.7536C>G
XR_940372.1:n.7510C>G
XM_017005688.1:c.7413C>G	XP_016861177.1:p.Pro2471=
XM_017005689.1:c.7473C>G	XP_016861178.1:p.Pro2491=
XM_017005692.1:c.*28C>G	XP_016861181.1:n.*28C>G
XR_001740003.1:n.7509C>G
XR_001740004.1:n.7509C>G
XR_001740005.1:n.7509C>G
XR_001740006.1:n.7483C>G
NM_000094.4:c.7473C>G MANE Select	NP_000085.1:p.Pro2491=