Canonical Allele Identifier: CA352641290
Gene: COL7A1 HGNC NCBI

Linked Data

gnomAD v4: 3-48567733-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48567733G>T , CM000665.2:g.48567733G>T GRCh38
NC_000003.11:g.48605166G>T , CM000665.1:g.48605166G>T GRCh37
NC_000003.10:g.48580170G>T NCBI36
NG_007065.1:g.32520C>A , LRG_286:g.32520C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.7960C>A MANE Select ENSP00000506558.1:p.Leu2654Met
ENST00000328333.12:c.7960C>A ENSP00000332371.8:p.Leu2654Met
ENST00000459756.5:n.783C>A
ENST00000487017.5:n.4599C>A
NM_000094.3:c.7960C>A , LRG_286t1:c.7960C>A NP_000085.1:p.Leu2654Met
XM_011533336.1:c.7987C>A XP_011531638.1:p.Leu2663Met
XM_011533337.1:c.7960C>A XP_011531639.1:p.Leu2654Met
XM_011533338.1:c.7927C>A XP_011531640.1:p.Leu2643Met
XR_940369.1:n.8023C>A
XR_940370.1:n.8023C>A
XR_940371.1:n.8023C>A
XM_017005688.1:c.7900C>A XP_016861177.1:p.Leu2634Met
XR_001740003.1:n.7996C>A
XR_001740004.1:n.7996C>A
XR_001740005.1:n.7996C>A
NM_000094.4:c.7960C>A MANE Select NP_000085.1:p.Leu2654Met