Canonical Allele Identifier: CA7047940
Community Standard Title: NM_001845.6(COL4A1):c.1426C>T (p.Arg476Trp)
Gene: COL4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110192869G>A , CM000675.2:g.110192869G>A GRCh38
NC_000013.10:g.110845216G>A , CM000675.1:g.110845216G>A GRCh37
NC_000013.9:g.109643217G>A NCBI36
NG_011544.2:g.119281C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001845.6:c.1426C>T MANE Select NP_001836.3:p.Arg476Trp
ENST00000375820.10:c.1426C>T MANE Select ENSP00000364979.4:p.Arg476Trp
NM_001303110.1:c.1426C>T NP_001290039.1:p.Arg476Trp
NM_001303110.2:c.1426C>T NP_001290039.1:p.Arg476Trp
NM_001845.5:c.1426C>T NP_001836.3:p.Arg476Trp
ENST00000375820.8:c.1426C>T ENSP00000364979.4:p.Arg476Trp
ENST00000543140.5:c.1426C>T ENSP00000443348.1:p.Arg476Trp
ENST00000543140.6:c.1426C>T ENSP00000443348.1:p.Arg476Trp
ENST00000649738.1:n.1556C>T
XM_011521048.1:c.1234C>T XP_011519350.1:p.Arg412Trp
XM_011521048.2:c.1234C>T XP_011519350.1:p.Arg412Trp