Canonical Allele Identifier: CA1363075445
Gene: COL7A1 HGNC NCBI

Linked Data

dbSNP Id: rs2043652111
gnomAD v4: 3-48567348-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48567348C>T , CM000665.2:g.48567348C>T GRCh38
NC_000003.11:g.48604781C>T , CM000665.1:g.48604781C>T GRCh37
NC_000003.10:g.48579785C>T NCBI36
NG_007065.1:g.32905G>A , LRG_286:g.32905G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.8047-158G>A MANE Select ENSP00000506558.1:n.8047-158G>A
ENST00000328333.12:c.8047-158G>A ENSP00000332371.8:n.8047-158G>A
ENST00000474432.1:n.16G>A
ENST00000487017.5:n.4686-158G>A
NM_000094.3:c.8047-158G>A , LRG_286t1:c.8047-158G>A NP_000085.1:n.8047-158G>A
XM_011533336.1:c.8074-158G>A XP_011531638.1:n.8074-158G>A
XM_011533337.1:c.8047-158G>A XP_011531639.1:n.8047-158G>A
XM_011533338.1:c.8014-158G>A XP_011531640.1:n.8014-158G>A
XR_940369.1:n.8110-158G>A
XR_940370.1:n.8110-158G>A
XR_940371.1:n.8110-158G>A
XM_017005688.1:c.7987-158G>A XP_016861177.1:n.7987-158G>A
XR_001740003.1:n.8083-158G>A
XR_001740004.1:n.8083-158G>A
XR_001740005.1:n.8083-158G>A
NM_000094.4:c.8047-158G>A MANE Select NP_000085.1:n.8047-158G>A