Canonical Allele Identifier: CA352642260

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48605961G>T (hg19) ; chr3:g.48568528G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568528G>T , CM000665.2:g.48568528G>T	GRCh38
NC_000003.11:g.48605961G>T , CM000665.1:g.48605961G>T	GRCh37
NC_000003.10:g.48580965G>T	NCBI36
NG_007065.1:g.31725C>A , LRG_286:g.31725C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7765C>A MANE Select	ENSP00000506558.1:p.Pro2589Thr
ENST00000328333.12:c.7765C>A	ENSP00000332371.8:p.Pro2589Thr
ENST00000459756.5:n.588C>A
ENST00000467985.1:n.611C>A
ENST00000487017.5:n.4404C>A
NM_000094.3:c.7765C>A , LRG_286t1:c.7765C>A	NP_000085.1:p.Pro2589Thr
XM_011533336.1:c.7792C>A	XP_011531638.1:p.Pro2598Thr
XM_011533337.1:c.7765C>A	XP_011531639.1:p.Pro2589Thr
XM_011533338.1:c.7732C>A	XP_011531640.1:p.Pro2578Thr
XM_011533339.1:c.7792C>A	XP_011531641.1:p.Pro2598Thr
XR_940369.1:n.7828C>A
XR_940370.1:n.7828C>A
XR_940371.1:n.7828C>A
XR_940372.1:n.7802C>A
XM_017005688.1:c.7705C>A	XP_016861177.1:p.Pro2569Thr
XM_017005689.1:c.7765C>A	XP_016861178.1:p.Pro2589Thr
XR_001740003.1:n.7801C>A
XR_001740004.1:n.7801C>A
XR_001740005.1:n.7801C>A
XR_001740006.1:n.7775C>A
NM_000094.4:c.7765C>A MANE Select	NP_000085.1:p.Pro2589Thr