Canonical Allele Identifier: CA2450712993
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108668503_108668504delinsAG , CM000685.2:g.108668503_108668504delinsAG GRCh38
NC_000023.10:g.107911733_107911734delinsAG , CM000685.1:g.107911733_107911734delinsAG GRCh37
NC_000023.9:g.107798389_107798390delinsAG NCBI36
NG_011977.1:g.233580_233581delinsAG
NG_011977.2:g.233580_233581delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.3789_3790delinsAG MANE Select ENSP00000331902.7:p.Pro1263=
ENST00000361603.7:c.3789_3790delinsAG ENSP00000354505.2:p.Pro1263=
ENST00000328300.10:c.3789_3790delinsAG ENSP00000331902.6:p.Pro1263=
ENST00000361603.6:c.3789_3790delinsAG ENSP00000354505.2:p.Pro1263=
NM_000495.4:c.3789_3790delinsAG NP_000486.1:p.Pro1263=
NM_033380.2:c.3789_3790delinsAG NP_203699.1:p.Pro1263=
XM_005262070.2:c.3789_3790delinsAG XP_005262127.1:p.Pro1263=
XM_006724616.2:c.3789_3790delinsAG XP_006724679.1:p.Pro1263=
XM_011530849.1:c.3465_3466delinsAG XP_011529151.1:p.Pro1155=
XM_011530850.1:c.3789_3790delinsAG XP_011529152.1:p.Pro1263=
XM_011530851.1:c.1362_1363delinsAG XP_011529153.1:p.Pro454=
XM_011530849.2:c.3804_3805delinsAG XP_011529151.2:p.Pro1268=
XM_017029259.2:c.3804_3805delinsAG XP_016884748.1:p.Pro1268=
XM_017029260.1:c.3804_3805delinsAG XP_016884749.1:p.Pro1268=
XM_017029261.1:c.3804_3805delinsAG XP_016884750.1:p.Pro1268=
XM_017029262.2:c.3804_3805delinsAG XP_016884751.1:p.Pro1268=
XM_017029263.2:c.2124_2125delinsAG XP_016884752.1:p.Pro708=
NM_000495.5:c.3789_3790delinsAG NP_000486.1:p.Pro1263=
NM_033380.3:c.3789_3790delinsAG MANE Select NP_203699.1:p.Pro1263=