Canonical Allele Identifier: CA352637197

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48604091A>T (hg19) ; chr3:g.48566658A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48566658A>T , CM000665.2:g.48566658A>T	GRCh38
NC_000003.11:g.48604091A>T , CM000665.1:g.48604091A>T	GRCh37
NC_000003.10:g.48579095A>T	NCBI36
NG_007065.1:g.33595T>A , LRG_286:g.33595T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.8304+2T>A MANE Select	ENSP00000506558.1:n.8304+2T>A
ENST00000328333.12:c.8304+2T>A	ENSP00000332371.8:n.8304+2T>A
ENST00000474432.1:n.704+2T>A
ENST00000487017.5:n.4943+2T>A
NM_000094.3:c.8304+2T>A , LRG_286t1:c.8304+2T>A	NP_000085.1:n.8304+2T>A
XM_011533336.1:c.8331+2T>A	XP_011531638.1:n.8331+2T>A
XM_011533337.1:c.8304+2T>A	XP_011531639.1:n.8304+2T>A
XM_011533338.1:c.8271+2T>A	XP_011531640.1:n.8271+2T>A
XR_940369.1:n.8367+2T>A
XR_940370.1:n.8367+2T>A
XR_940371.1:n.8367+2T>A
XM_017005688.1:c.8244+2T>A	XP_016861177.1:n.8244+2T>A
XR_001740003.1:n.8340+2T>A
XR_001740004.1:n.8340+2T>A
XR_001740005.1:n.8340+2T>A
NM_000094.4:c.8304+2T>A MANE Select	NP_000085.1:n.8304+2T>A