Canonical Allele Identifier: CA352641350

Gene: COL7A1

Linked Data

• dbSNP Id: rs2043671687
• gnomAD v3: 3-48567748-G-T
• gnomAD v4: 3-48567748-G-T
• MyVariant Identifiers: chr3:g.48605181G>T (hg19) ; chr3:g.48567748G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48567748G>T , CM000665.2:g.48567748G>T	GRCh38
NC_000003.11:g.48605181G>T , CM000665.1:g.48605181G>T	GRCh37
NC_000003.10:g.48580185G>T	NCBI36
NG_007065.1:g.32505C>A , LRG_286:g.32505C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7945C>A MANE Select	ENSP00000506558.1:p.Pro2649Thr
ENST00000328333.12:c.7945C>A	ENSP00000332371.8:p.Pro2649Thr
ENST00000459756.5:n.768C>A
ENST00000487017.5:n.4584C>A
NM_000094.3:c.7945C>A , LRG_286t1:c.7945C>A	NP_000085.1:p.Pro2649Thr
XM_011533336.1:c.7972C>A	XP_011531638.1:p.Pro2658Thr
XM_011533337.1:c.7945C>A	XP_011531639.1:p.Pro2649Thr
XM_011533338.1:c.7912C>A	XP_011531640.1:p.Pro2638Thr
XR_940369.1:n.8008C>A
XR_940370.1:n.8008C>A
XR_940371.1:n.8008C>A
XM_017005688.1:c.7885C>A	XP_016861177.1:p.Pro2629Thr
XR_001740003.1:n.7981C>A
XR_001740004.1:n.7981C>A
XR_001740005.1:n.7981C>A
NM_000094.4:c.7945C>A MANE Select	NP_000085.1:p.Pro2649Thr