Canonical Allele Identifier: CA352636249

Gene: COL7A1

Linked Data

• gnomAD v4: 3-48566283-C-A
• MyVariant Identifiers: chr3:g.48603716C>A (hg19) ; chr3:g.48566283C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48566283C>A , CM000665.2:g.48566283C>A	GRCh38
NC_000003.11:g.48603716C>A , CM000665.1:g.48603716C>A	GRCh37
NC_000003.10:g.48578720C>A	NCBI36
NG_007065.1:g.33970G>T , LRG_286:g.33970G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.8391G>T MANE Select	ENSP00000506558.1:p.Glu2797Asp
ENST00000328333.12:c.8391G>T	ENSP00000332371.8:p.Glu2797Asp
ENST00000487017.5:n.5030G>T
NM_000094.3:c.8391G>T , LRG_286t1:c.8391G>T	NP_000085.1:p.Glu2797Asp
XM_011533336.1:c.8418G>T	XP_011531638.1:p.Glu2806Asp
XM_011533337.1:c.8391G>T	XP_011531639.1:p.Glu2797Asp
XM_011533338.1:c.8358G>T	XP_011531640.1:p.Glu2786Asp
XR_940369.1:n.8454G>T
XR_940370.1:n.8454G>T
XR_940371.1:n.8454G>T
XM_017005688.1:c.8331G>T	XP_016861177.1:p.Glu2777Asp
XR_001740003.1:n.8427G>T
XR_001740004.1:n.8427G>T
XR_001740005.1:n.8427G>T
NM_000094.4:c.8391G>T MANE Select	NP_000085.1:p.Glu2797Asp