Canonical Allele Identifier: CA2378335
Gene: COL7A1 HGNC NCBI

Linked Data

dbSNP Id: rs760096740
gnomAD v2: 3-48606222-G-A
gnomAD v4: 3-48568789-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48568789G>A , CM000665.2:g.48568789G>A GRCh38
NC_000003.11:g.48606222G>A , CM000665.1:g.48606222G>A GRCh37
NC_000003.10:g.48581226G>A NCBI36
NG_007065.1:g.31464C>T , LRG_286:g.31464C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.7753C>T MANE Select ENSP00000506558.1:p.Pro2585Ser
ENST00000328333.12:c.7753C>T ENSP00000332371.8:p.Pro2585Ser
ENST00000459756.5:n.576C>T
ENST00000467985.1:n.599C>T
ENST00000487017.5:n.4392C>T
NM_000094.3:c.7753C>T , LRG_286t1:c.7753C>T NP_000085.1:p.Pro2585Ser
XM_011533336.1:c.7780C>T XP_011531638.1:p.Pro2594Ser
XM_011533337.1:c.7753C>T XP_011531639.1:p.Pro2585Ser
XM_011533338.1:c.7720C>T XP_011531640.1:p.Pro2574Ser
XM_011533339.1:c.7780C>T XP_011531641.1:p.Pro2594Ser
XR_940369.1:n.7816C>T
XR_940370.1:n.7816C>T
XR_940371.1:n.7816C>T
XR_940372.1:n.7790C>T
XM_017005688.1:c.7693C>T XP_016861177.1:p.Pro2565Ser
XM_017005689.1:c.7753C>T XP_016861178.1:p.Pro2585Ser
XR_001740003.1:n.7789C>T
XR_001740004.1:n.7789C>T
XR_001740005.1:n.7789C>T
XR_001740006.1:n.7763C>T
NM_000094.4:c.7753C>T MANE Select NP_000085.1:p.Pro2585Ser