Canonical Allele Identifier: CA2577587661
Gene: COL7A1 HGNC NCBI

Linked Data

gnomAD v4: 3-48568185-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48568185G>A , CM000665.2:g.48568185G>A GRCh38
NC_000003.11:g.48605618G>A , CM000665.1:g.48605618G>A GRCh37
NC_000003.10:g.48580622G>A NCBI36
NG_007065.1:g.32068C>T , LRG_286:g.32068C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.7795-15C>T MANE Select ENSP00000506558.1:n.7795-15C>T
ENST00000328333.12:c.7795-15C>T ENSP00000332371.8:n.7795-15C>T
ENST00000459756.5:n.618-15C>T
ENST00000467985.1:n.688C>T
ENST00000487017.5:n.4434-15C>T
NM_000094.3:c.7795-15C>T , LRG_286t1:c.7795-15C>T NP_000085.1:n.7795-15C>T
XM_011533336.1:c.7822-15C>T XP_011531638.1:n.7822-15C>T
XM_011533337.1:c.7795-15C>T XP_011531639.1:n.7795-15C>T
XM_011533338.1:c.7762-15C>T XP_011531640.1:n.7762-15C>T
XM_011533339.1:c.*12C>T XP_011531641.1:n.*12C>T
XR_940369.1:n.7858-15C>T
XR_940370.1:n.7858-15C>T
XR_940371.1:n.7858-15C>T
XR_940372.1:n.7832-15C>T
XM_017005688.1:c.7735-15C>T XP_016861177.1:n.7735-15C>T
XM_017005689.1:c.*12C>T XP_016861178.1:n.*12C>T
XR_001740003.1:n.7831-15C>T
XR_001740004.1:n.7831-15C>T
XR_001740005.1:n.7831-15C>T
XR_001740006.1:n.7805-15C>T
NM_000094.4:c.7795-15C>T MANE Select NP_000085.1:n.7795-15C>T