Canonical Allele Identifier: CA388724802
Community Standard Title: NM_001845.6(COL4A1):c.868G>C (p.Gly290Arg)
Gene: COL4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110205529C>G , CM000675.2:g.110205529C>G GRCh38
NC_000013.10:g.110857876C>G , CM000675.1:g.110857876C>G GRCh37
NC_000013.9:g.109655877C>G NCBI36
NG_011544.2:g.106621G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001845.6:c.868G>C MANE Select NP_001836.3:p.Gly290Arg
ENST00000375820.10:c.868G>C MANE Select ENSP00000364979.4:p.Gly290Arg
NM_001303110.1:c.868G>C NP_001290039.1:p.Gly290Arg
NM_001303110.2:c.868G>C NP_001290039.1:p.Gly290Arg
NM_001845.5:c.868G>C NP_001836.3:p.Gly290Arg
ENST00000375820.8:c.868G>C ENSP00000364979.4:p.Gly290Arg
ENST00000543140.5:c.868G>C ENSP00000443348.1:p.Gly290Arg
ENST00000543140.6:c.868G>C ENSP00000443348.1:p.Gly290Arg
ENST00000615732.2:c.676G>C ENSP00000478222.2:p.Gly226Arg
ENST00000647632.1:n.501G>C
ENST00000647797.1:c.747G>C
ENST00000649738.1:n.998G>C
XM_011521048.1:c.676G>C XP_011519350.1:p.Gly226Arg
XM_011521048.2:c.676G>C XP_011519350.1:p.Gly226Arg