Canonical Allele Identifier: CA352640919

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48605008T>G (hg19) ; chr3:g.48567575T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48567575T>G , CM000665.2:g.48567575T>G	GRCh38
NC_000003.11:g.48605008T>G , CM000665.1:g.48605008T>G	GRCh37
NC_000003.10:g.48580012T>G	NCBI36
NG_007065.1:g.32678A>C , LRG_286:g.32678A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.8045A>C MANE Select	ENSP00000506558.1:p.Lys2682Thr
ENST00000328333.12:c.8045A>C	ENSP00000332371.8:p.Lys2682Thr
ENST00000487017.5:n.4684A>C
NM_000094.3:c.8045A>C , LRG_286t1:c.8045A>C	NP_000085.1:p.Lys2682Thr
XM_011533336.1:c.8072A>C	XP_011531638.1:p.Lys2691Thr
XM_011533337.1:c.8045A>C	XP_011531639.1:p.Lys2682Thr
XM_011533338.1:c.8012A>C	XP_011531640.1:p.Lys2671Thr
XR_940369.1:n.8108A>C
XR_940370.1:n.8108A>C
XR_940371.1:n.8108A>C
XM_017005688.1:c.7985A>C	XP_016861177.1:p.Lys2662Thr
XR_001740003.1:n.8081A>C
XR_001740004.1:n.8081A>C
XR_001740005.1:n.8081A>C
NM_000094.4:c.8045A>C MANE Select	NP_000085.1:p.Lys2682Thr