Canonical Allele Identifier: CA2450697613
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108626329C= , CM000685.2:g.108626329C= GRCh38
NC_000023.10:g.107869559C= , CM000685.1:g.107869559C= GRCh37
NC_000023.9:g.107756215C= NCBI36
NG_011977.1:g.191406C=
NG_011977.2:g.191406C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.3226C= MANE Select ENSP00000331902.7:p.Pro1076=
ENST00000361603.7:c.3226C= ENSP00000354505.2:p.Pro1076=
ENST00000328300.10:c.3226C= ENSP00000331902.6:p.Pro1076=
ENST00000361603.6:c.3226C= ENSP00000354505.2:p.Pro1076=
ENST00000483338.1:n.2682C=
ENST00000505728.1:c.459C=
NM_000495.4:c.3226C= NP_000486.1:p.Pro1076=
NM_033380.2:c.3226C= NP_203699.1:p.Pro1076=
XM_005262070.2:c.3226C= XP_005262127.1:p.Pro1076=
XM_005262072.3:c.3226C= XP_005262129.1:p.Pro1076=
XM_006724616.2:c.3226C= XP_006724679.1:p.Pro1076=
XM_011530849.1:c.2902C= XP_011529151.1:p.Pro968=
XM_011530850.1:c.3226C= XP_011529152.1:p.Pro1076=
XM_011530851.1:c.799C= XP_011529153.1:p.Pro267=
XM_011530849.2:c.3241C= XP_011529151.2:p.Pro1081=
XM_017029259.2:c.3241C= XP_016884748.1:p.Pro1081=
XM_017029260.1:c.3241C= XP_016884749.1:p.Pro1081=
XM_017029261.1:c.3241C= XP_016884750.1:p.Pro1081=
XM_017029262.2:c.3241C= XP_016884751.1:p.Pro1081=
XM_017029263.2:c.1561C= XP_016884752.1:p.Pro521=
NM_000495.5:c.3226C= NP_000486.1:p.Pro1076=
NM_033380.3:c.3226C= MANE Select NP_203699.1:p.Pro1076=