Canonical Allele Identifier: CA413849159
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108606862A>C , CM000685.2:g.108606862A>C GRCh38
NC_000023.10:g.107850092A>C , CM000685.1:g.107850092A>C GRCh37
NC_000023.9:g.107736748A>C NCBI36
NG_011977.1:g.171939A>C
NG_011977.2:g.171939A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.2365A>C MANE Select ENSP00000331902.7:p.Thr789Pro
ENST00000361603.7:c.2365A>C ENSP00000354505.2:p.Thr789Pro
ENST00000328300.10:c.2365A>C ENSP00000331902.6:p.Thr789Pro
ENST00000361603.6:c.2365A>C ENSP00000354505.2:p.Thr789Pro
ENST00000483338.1:n.1821A>C
NM_000495.4:c.2365A>C NP_000486.1:p.Thr789Pro
NM_033380.2:c.2365A>C NP_203699.1:p.Thr789Pro
XM_005262070.2:c.2365A>C XP_005262127.1:p.Thr789Pro
XM_005262072.3:c.2365A>C XP_005262129.1:p.Thr789Pro
XM_006724616.2:c.2365A>C XP_006724679.1:p.Thr789Pro
XM_011530849.1:c.2041A>C XP_011529151.1:p.Thr681Pro
XM_011530850.1:c.2365A>C XP_011529152.1:p.Thr789Pro
XM_011530851.1:c.-33+3801A>C XP_011529153.1:n.-33+3801A>C
XM_011530849.2:c.2380A>C XP_011529151.2:p.Thr794Pro
XM_017029259.2:c.2380A>C XP_016884748.1:p.Thr794Pro
XM_017029260.1:c.2380A>C XP_016884749.1:p.Thr794Pro
XM_017029261.1:c.2380A>C XP_016884750.1:p.Thr794Pro
XM_017029262.2:c.2380A>C XP_016884751.1:p.Thr794Pro
XM_017029263.2:c.700A>C XP_016884752.1:p.Thr234Pro
NM_000495.5:c.2365A>C NP_000486.1:p.Thr789Pro
NM_033380.3:c.2365A>C MANE Select NP_203699.1:p.Thr789Pro