Canonical Allele Identifier: CA2577587652
Gene: COL7A1 HGNC NCBI

Linked Data

gnomAD v4: 3-48568006-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48568006G>A , CM000665.2:g.48568006G>A GRCh38
NC_000003.11:g.48605439G>A , CM000665.1:g.48605439G>A GRCh37
NC_000003.10:g.48580443G>A NCBI36
NG_007065.1:g.32247C>T , LRG_286:g.32247C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.7875+84C>T MANE Select ENSP00000506558.1:n.7875+84C>T
ENST00000328333.12:c.7875+84C>T ENSP00000332371.8:n.7875+84C>T
ENST00000459756.5:n.698+84C>T
ENST00000487017.5:n.4514+84C>T
NM_000094.3:c.7875+84C>T , LRG_286t1:c.7875+84C>T NP_000085.1:n.7875+84C>T
XM_011533336.1:c.7902+84C>T XP_011531638.1:n.7902+84C>T
XM_011533337.1:c.7875+84C>T XP_011531639.1:n.7875+84C>T
XM_011533338.1:c.7842+84C>T XP_011531640.1:n.7842+84C>T
XR_940369.1:n.7938+84C>T
XR_940370.1:n.7938+84C>T
XR_940371.1:n.7938+84C>T
XM_017005688.1:c.7815+84C>T XP_016861177.1:n.7815+84C>T
XR_001740003.1:n.7911+84C>T
XR_001740004.1:n.7911+84C>T
XR_001740005.1:n.7911+84C>T
NM_000094.4:c.7875+84C>T MANE Select NP_000085.1:n.7875+84C>T