Canonical Allele Identifier: CA7048056
Community Standard Title: NM_001845.6(COL4A1):c.1092A>T (p.Pro364=)
Gene: COL4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110200882T>A , CM000675.2:g.110200882T>A GRCh38
NC_000013.10:g.110853229T>A , CM000675.1:g.110853229T>A GRCh37
NC_000013.9:g.109651230T>A NCBI36
NG_011544.2:g.111268A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001845.6:c.1092A>T MANE Select NP_001836.3:p.Pro364=
ENST00000375820.10:c.1092A>T MANE Select ENSP00000364979.4:p.Pro364=
NM_001303110.1:c.1092A>T NP_001290039.1:p.Pro364=
NM_001303110.2:c.1092A>T NP_001290039.1:p.Pro364=
NM_001845.5:c.1092A>T NP_001836.3:p.Pro364=
ENST00000375820.8:c.1092A>T ENSP00000364979.4:p.Pro364=
ENST00000543140.5:c.1092A>T ENSP00000443348.1:p.Pro364=
ENST00000543140.6:c.1092A>T ENSP00000443348.1:p.Pro364=
ENST00000647797.1:c.971A>T
ENST00000649738.1:n.1222A>T
XM_011521048.1:c.900A>T XP_011519350.1:p.Pro300=
XM_011521048.2:c.900A>T XP_011519350.1:p.Pro300=