Canonical Allele Identifier: CA2665615701

Gene: COL7A1

Linked Data

• gnomAD v4: 3-48565537-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48565537A>C , CM000665.2:g.48565537A>C	GRCh38
NC_000003.11:g.48602970A>C , CM000665.1:g.48602970A>C	GRCh37
NC_000003.10:g.48577974A>C	NCBI36
NG_007065.1:g.34716T>G , LRG_286:g.34716T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.8441-41T>G MANE Select	ENSP00000506558.1:n.8441-41T>G
ENST00000328333.12:c.8441-41T>G	ENSP00000332371.8:n.8441-41T>G
ENST00000487017.5:n.5080-41T>G
NM_000094.3:c.8441-41T>G , LRG_286t1:c.8441-41T>G	NP_000085.1:n.8441-41T>G
XM_011533336.1:c.8468-41T>G	XP_011531638.1:n.8468-41T>G
XM_011533337.1:c.8441-41T>G	XP_011531639.1:n.8441-41T>G
XM_011533338.1:c.8408-41T>G	XP_011531640.1:n.8408-41T>G
XR_940369.1:n.8504-41T>G
XR_940370.1:n.8504-41T>G
XR_940371.1:n.8504-41T>G
XM_017005688.1:c.8381-41T>G	XP_016861177.1:n.8381-41T>G
XR_001740003.1:n.8477-41T>G
XR_001740004.1:n.8477-41T>G
XR_001740005.1:n.8477-41T>G
NM_000094.4:c.8441-41T>G MANE Select	NP_000085.1:n.8441-41T>G