Canonical Allele Identifier: CA73970284

Gene: COL7A1

Linked Data

• dbSNP Id: rs1051795889
• gnomAD v3: 3-48565556-A-G
• gnomAD v4: 3-48565556-A-G
• MyVariant Identifiers: chr3:g.48602989A>G (hg19) ; chr3:g.48565556A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48565556A>G , CM000665.2:g.48565556A>G	GRCh38
NC_000003.11:g.48602989A>G , CM000665.1:g.48602989A>G	GRCh37
NC_000003.10:g.48577993A>G	NCBI36
NG_007065.1:g.34697T>C , LRG_286:g.34697T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.8441-60T>C MANE Select	ENSP00000506558.1:n.8441-60T>C
ENST00000328333.12:c.8441-60T>C	ENSP00000332371.8:n.8441-60T>C
ENST00000487017.5:n.5080-60T>C
NM_000094.3:c.8441-60T>C , LRG_286t1:c.8441-60T>C	NP_000085.1:n.8441-60T>C
XM_011533336.1:c.8468-60T>C	XP_011531638.1:n.8468-60T>C
XM_011533337.1:c.8441-60T>C	XP_011531639.1:n.8441-60T>C
XM_011533338.1:c.8408-60T>C	XP_011531640.1:n.8408-60T>C
XR_940369.1:n.8504-60T>C
XR_940370.1:n.8504-60T>C
XR_940371.1:n.8504-60T>C
XM_017005688.1:c.8381-60T>C	XP_016861177.1:n.8381-60T>C
XR_001740003.1:n.8477-60T>C
XR_001740004.1:n.8477-60T>C
XR_001740005.1:n.8477-60T>C
NM_000094.4:c.8441-60T>C MANE Select	NP_000085.1:n.8441-60T>C