Canonical Allele Identifier: CA352641182

Gene: COL7A1

Linked Data

• dbSNP Id: rs2043665076
• gnomAD v4: 3-48567630-G-A
• MyVariant Identifiers: chr3:g.48605063G>A (hg19) ; chr3:g.48567630G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48567630G>A , CM000665.2:g.48567630G>A	GRCh38
NC_000003.11:g.48605063G>A , CM000665.1:g.48605063G>A	GRCh37
NC_000003.10:g.48580067G>A	NCBI36
NG_007065.1:g.32623C>T , LRG_286:g.32623C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7990C>T MANE Select	ENSP00000506558.1:p.Pro2664Ser
ENST00000328333.12:c.7990C>T	ENSP00000332371.8:p.Pro2664Ser
ENST00000487017.5:n.4629C>T
NM_000094.3:c.7990C>T , LRG_286t1:c.7990C>T	NP_000085.1:p.Pro2664Ser
XM_011533336.1:c.8017C>T	XP_011531638.1:p.Pro2673Ser
XM_011533337.1:c.7990C>T	XP_011531639.1:p.Pro2664Ser
XM_011533338.1:c.7957C>T	XP_011531640.1:p.Pro2653Ser
XR_940369.1:n.8053C>T
XR_940370.1:n.8053C>T
XR_940371.1:n.8053C>T
XM_017005688.1:c.7930C>T	XP_016861177.1:p.Pro2644Ser
XR_001740003.1:n.8026C>T
XR_001740004.1:n.8026C>T
XR_001740005.1:n.8026C>T
NM_000094.4:c.7990C>T MANE Select	NP_000085.1:p.Pro2664Ser