Canonical Allele Identifier: CA352641472

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48605275T>A (hg19) ; chr3:g.48567842T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48567842T>A , CM000665.2:g.48567842T>A	GRCh38
NC_000003.11:g.48605275T>A , CM000665.1:g.48605275T>A	GRCh37
NC_000003.10:g.48580279T>A	NCBI36
NG_007065.1:g.32411A>T , LRG_286:g.32411A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7925A>T MANE Select	ENSP00000506558.1:p.Asp2642Val
ENST00000328333.12:c.7925A>T	ENSP00000332371.8:p.Asp2642Val
ENST00000459756.5:n.748A>T
ENST00000487017.5:n.4564A>T
NM_000094.3:c.7925A>T , LRG_286t1:c.7925A>T	NP_000085.1:p.Asp2642Val
XM_011533336.1:c.7952A>T	XP_011531638.1:p.Asp2651Val
XM_011533337.1:c.7925A>T	XP_011531639.1:p.Asp2642Val
XM_011533338.1:c.7892A>T	XP_011531640.1:p.Asp2631Val
XR_940369.1:n.7988A>T
XR_940370.1:n.7988A>T
XR_940371.1:n.7988A>T
XM_017005688.1:c.7865A>T	XP_016861177.1:p.Asp2622Val
XR_001740003.1:n.7961A>T
XR_001740004.1:n.7961A>T
XR_001740005.1:n.7961A>T
NM_000094.4:c.7925A>T MANE Select	NP_000085.1:p.Asp2642Val