Canonical Allele Identifier: CA352641919
Gene: COL7A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48568127T>C , CM000665.2:g.48568127T>C GRCh38
NC_000003.11:g.48605560T>C , CM000665.1:g.48605560T>C GRCh37
NC_000003.10:g.48580564T>C NCBI36
NG_007065.1:g.32126A>G , LRG_286:g.32126A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.7838A>G MANE Select ENSP00000506558.1:p.Lys2613Arg
ENST00000328333.12:c.7838A>G ENSP00000332371.8:p.Lys2613Arg
ENST00000459756.5:n.661A>G
ENST00000487017.5:n.4477A>G
NM_000094.3:c.7838A>G , LRG_286t1:c.7838A>G NP_000085.1:p.Lys2613Arg
XM_011533336.1:c.7865A>G XP_011531638.1:p.Lys2622Arg
XM_011533337.1:c.7838A>G XP_011531639.1:p.Lys2613Arg
XM_011533338.1:c.7805A>G XP_011531640.1:p.Lys2602Arg
XR_940369.1:n.7901A>G
XR_940370.1:n.7901A>G
XR_940371.1:n.7901A>G
XM_017005688.1:c.7778A>G XP_016861177.1:p.Lys2593Arg
XR_001740003.1:n.7874A>G
XR_001740004.1:n.7874A>G
XR_001740005.1:n.7874A>G
NM_000094.4:c.7838A>G MANE Select NP_000085.1:p.Lys2613Arg