Canonical Allele Identifier: CA352642066

Gene: COL7A1

Linked Data

• gnomAD v4: 3-48568164-G-A
• MyVariant Identifiers: chr3:g.48605597G>A (hg19) ; chr3:g.48568164G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568164G>A , CM000665.2:g.48568164G>A	GRCh38
NC_000003.11:g.48605597G>A , CM000665.1:g.48605597G>A	GRCh37
NC_000003.10:g.48580601G>A	NCBI36
NG_007065.1:g.32089C>T , LRG_286:g.32089C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7801C>T MANE Select	ENSP00000506558.1:p.Pro2601Ser
ENST00000328333.12:c.7801C>T	ENSP00000332371.8:p.Pro2601Ser
ENST00000459756.5:n.624C>T
ENST00000467985.1:n.709C>T
ENST00000487017.5:n.4440C>T
NM_000094.3:c.7801C>T , LRG_286t1:c.7801C>T	NP_000085.1:p.Pro2601Ser
XM_011533336.1:c.7828C>T	XP_011531638.1:p.Pro2610Ser
XM_011533337.1:c.7801C>T	XP_011531639.1:p.Pro2601Ser
XM_011533338.1:c.7768C>T	XP_011531640.1:p.Pro2590Ser
XM_011533339.1:c.*33C>T	XP_011531641.1:n.*33C>T
XR_940369.1:n.7864C>T
XR_940370.1:n.7864C>T
XR_940371.1:n.7864C>T
XR_940372.1:n.7838C>T
XM_017005688.1:c.7741C>T	XP_016861177.1:p.Pro2581Ser
XM_017005689.1:c.*33C>T	XP_016861178.1:n.*33C>T
XR_001740003.1:n.7837C>T
XR_001740004.1:n.7837C>T
XR_001740005.1:n.7837C>T
XR_001740006.1:n.7811C>T
NM_000094.4:c.7801C>T MANE Select	NP_000085.1:p.Pro2601Ser