Canonical Allele Identifier: CA352663105

Gene: COL7A1

Linked Data

• ClinVar Variation Id: 1481070
• ClinVar RCV Id: RCV001988224
• dbSNP Id: rs2107674241
• MyVariant Identifiers: chr3:g.48612831T>C (hg19) ; chr3:g.48575398T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48575398T>C , CM000665.2:g.48575398T>C	GRCh38
NC_000003.11:g.48612831T>C , CM000665.1:g.48612831T>C	GRCh37
NC_000003.10:g.48587835T>C	NCBI36
NG_007065.1:g.24855A>G , LRG_286:g.24855A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.6121A>G MANE Select	ENSP00000506558.1:p.Ile2041Val
ENST00000328333.12:c.6121A>G	ENSP00000332371.8:p.Ile2041Val
ENST00000487017.5:n.2038A>G
NM_000094.3:c.6121A>G , LRG_286t1:c.6121A>G	NP_000085.1:p.Ile2041Val
XM_011533336.1:c.6148A>G	XP_011531638.1:p.Ile2050Val
XM_011533337.1:c.6121A>G	XP_011531639.1:p.Ile2041Val
XM_011533338.1:c.6148A>G	XP_011531640.1:p.Ile2050Val
XM_011533339.1:c.6148A>G	XP_011531641.1:p.Ile2050Val
XM_011533340.1:c.6148A>G	XP_011531642.1:p.Ile2050Val
XM_011533341.1:c.6148A>G	XP_011531643.1:p.Ile2050Val
XM_011533342.1:c.6148A>G	XP_011531644.1:p.Ile2050Val
XR_940369.1:n.6184A>G
XR_940370.1:n.6184A>G
XR_940371.1:n.6184A>G
XR_940372.1:n.6184A>G
XR_940373.1:n.6184A>G
XR_940374.1:n.6184A>G
XR_940375.1:n.6181+3A>G
XM_017005688.1:c.6121A>G	XP_016861177.1:p.Ile2041Val
XM_017005689.1:c.6121A>G	XP_016861178.1:p.Ile2041Val
XM_017005690.1:c.6121A>G	XP_016861179.1:p.Ile2041Val
XM_017005691.1:c.6121A>G	XP_016861180.1:p.Ile2041Val
XM_017005692.1:c.6121A>G	XP_016861181.1:p.Ile2041Val
XR_001740003.1:n.6157A>G
XR_001740004.1:n.6157A>G
XR_001740005.1:n.6157A>G
XR_001740006.1:n.6157A>G
XR_001740007.1:n.6157A>G
XR_001740008.1:n.6157A>G
XR_001740009.1:n.6154+3A>G
NM_000094.4:c.6121A>G MANE Select	NP_000085.1:p.Ile2041Val