Canonical Allele Identifier: CA2575473025
Gene: COL4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110205303G>A , CM000675.2:g.110205303G>A GRCh38
NC_000013.10:g.110857650G>A , CM000675.1:g.110857650G>A GRCh37
NC_000013.9:g.109655651G>A NCBI36
NG_011544.2:g.106847C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375820.10:c.957+50C>T MANE Select ENSP00000364979.4:n.957+50C>T
ENST00000543140.6:c.957+50C>T ENSP00000443348.1:n.957+50C>T
ENST00000647632.1:n.640C>T
ENST00000647797.1:c.836+50C>T
ENST00000649738.1:n.1087+50C>T
ENST00000375820.8:c.957+50C>T ENSP00000364979.4:n.957+50C>T
ENST00000543140.5:c.957+50C>T ENSP00000443348.1:n.957+50C>T
NM_001303110.1:c.957+50C>T NP_001290039.1:n.957+50C>T
NM_001845.5:c.957+50C>T NP_001836.3:n.957+50C>T
XM_011521048.1:c.765+50C>T XP_011519350.1:n.765+50C>T
XM_011521048.2:c.765+50C>T XP_011519350.1:n.765+50C>T
NM_001845.6:c.957+50C>T MANE Select NP_001836.3:n.957+50C>T
NM_001303110.2:c.957+50C>T NP_001290039.1:n.957+50C>T