Canonical Allele Identifier: CA352646526

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48607760G>A (hg19) ; chr3:g.48570327G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48570327G>A , CM000665.2:g.48570327G>A	GRCh38
NC_000003.11:g.48607760G>A , CM000665.1:g.48607760G>A	GRCh37
NC_000003.10:g.48582764G>A	NCBI36
NG_007065.1:g.29926C>T , LRG_286:g.29926C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7388C>T MANE Select	ENSP00000506558.1:p.Pro2463Leu
ENST00000328333.12:c.7388C>T	ENSP00000332371.8:p.Pro2463Leu
ENST00000422991.1:c.383C>T	ENSP00000391608.1:p.Pro128Leu
ENST00000459756.5:n.115C>T
ENST00000467985.1:n.138C>T
ENST00000487017.5:n.4027C>T
NM_000094.3:c.7388C>T , LRG_286t1:c.7388C>T	NP_000085.1:p.Pro2463Leu
XM_011533336.1:c.7415C>T	XP_011531638.1:p.Pro2472Leu
XM_011533337.1:c.7388C>T	XP_011531639.1:p.Pro2463Leu
XM_011533338.1:c.7407+138C>T	XP_011531640.1:n.7407+138C>T
XM_011533339.1:c.7415C>T	XP_011531641.1:p.Pro2472Leu
XM_011533340.1:c.7408-75C>T	XP_011531642.1:n.7408-75C>T
XM_011533341.1:c.7382-75C>T	XP_011531643.1:n.7382-75C>T
XM_011533342.1:c.7381+138C>T	XP_011531644.1:n.7381+138C>T
XR_940369.1:n.7451C>T
XR_940370.1:n.7451C>T
XR_940371.1:n.7451C>T
XR_940372.1:n.7425C>T
XM_017005688.1:c.7380+138C>T	XP_016861177.1:n.7380+138C>T
XM_017005689.1:c.7388C>T	XP_016861178.1:p.Pro2463Leu
XM_017005690.1:c.7381-75C>T	XP_016861179.1:n.7381-75C>T
XM_017005691.1:c.7355-75C>T	XP_016861180.1:n.7355-75C>T
XM_017005692.1:c.7354+138C>T	XP_016861181.1:n.7354+138C>T
XR_001740003.1:n.7424C>T
XR_001740004.1:n.7424C>T
XR_001740005.1:n.7424C>T
XR_001740006.1:n.7398C>T
NM_000094.4:c.7388C>T MANE Select	NP_000085.1:p.Pro2463Leu