Canonical Allele Identifier: CA73970640

Gene: COL7A1

Linked Data

• dbSNP Id: rs112611395
• MyVariant Identifiers: chr3:g.48603750T>A (hg19) ; chr3:g.48566317T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48566317T>A , CM000665.2:g.48566317T>A	GRCh38
NC_000003.11:g.48603750T>A , CM000665.1:g.48603750T>A	GRCh37
NC_000003.10:g.48578754T>A	NCBI36
NG_007065.1:g.33936A>T , LRG_286:g.33936A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.8359-2A>T MANE Select	ENSP00000506558.1:n.8359-2A>T
ENST00000328333.12:c.8359-2A>T	ENSP00000332371.8:n.8359-2A>T
ENST00000487017.5:n.4998-2A>T
NM_000094.3:c.8359-2A>T , LRG_286t1:c.8359-2A>T	NP_000085.1:n.8359-2A>T
XM_011533336.1:c.8386-2A>T	XP_011531638.1:n.8386-2A>T
XM_011533337.1:c.8359-2A>T	XP_011531639.1:n.8359-2A>T
XM_011533338.1:c.8326-2A>T	XP_011531640.1:n.8326-2A>T
XR_940369.1:n.8422-2A>T
XR_940370.1:n.8422-2A>T
XR_940371.1:n.8422-2A>T
XM_017005688.1:c.8299-2A>T	XP_016861177.1:n.8299-2A>T
XR_001740003.1:n.8395-2A>T
XR_001740004.1:n.8395-2A>T
XR_001740005.1:n.8395-2A>T
NM_000094.4:c.8359-2A>T MANE Select	NP_000085.1:n.8359-2A>T