Canonical Allele Identifier: CA7048216
Community Standard Title: NM_001845.6(COL4A1):c.922G>A (p.Gly308Arg)
Gene: COL4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110205388C>T , CM000675.2:g.110205388C>T GRCh38
NC_000013.10:g.110857735C>T , CM000675.1:g.110857735C>T GRCh37
NC_000013.9:g.109655736C>T NCBI36
NG_011544.2:g.106762G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001845.6:c.922G>A MANE Select NP_001836.3:p.Gly308Arg
ENST00000375820.10:c.922G>A MANE Select ENSP00000364979.4:p.Gly308Arg
NM_001303110.1:c.922G>A NP_001290039.1:p.Gly308Arg
NM_001303110.2:c.922G>A NP_001290039.1:p.Gly308Arg
NM_001845.5:c.922G>A NP_001836.3:p.Gly308Arg
ENST00000375820.8:c.922G>A ENSP00000364979.4:p.Gly308Arg
ENST00000543140.5:c.922G>A ENSP00000443348.1:p.Gly308Arg
ENST00000543140.6:c.922G>A ENSP00000443348.1:p.Gly308Arg
ENST00000647632.1:n.555G>A
ENST00000647797.1:c.801G>A
ENST00000649738.1:n.1052G>A
XM_011521048.1:c.730G>A XP_011519350.1:p.Gly244Arg
XM_011521048.2:c.730G>A XP_011519350.1:p.Gly244Arg