Canonical Allele Identifier: CA2450712316
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108666512_108666513delinsTG , CM000685.2:g.108666512_108666513delinsTG GRCh38
NC_000023.10:g.107909742_107909743delinsTG , CM000685.1:g.107909742_107909743delinsTG GRCh37
NC_000023.9:g.107796398_107796399delinsTG NCBI36
NG_011977.1:g.231589_231590delinsTG
NG_011977.2:g.231589_231590delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.3471_3472delinsTG MANE Select ENSP00000331902.7:p.Pro1157=
ENST00000361603.7:c.3471_3472delinsTG ENSP00000354505.2:p.Pro1157=
ENST00000328300.10:c.3471_3472delinsTG ENSP00000331902.6:p.Pro1157=
ENST00000361603.6:c.3471_3472delinsTG ENSP00000354505.2:p.Pro1157=
NM_000495.4:c.3471_3472delinsTG NP_000486.1:p.Pro1157=
NM_033380.2:c.3471_3472delinsTG NP_203699.1:p.Pro1157=
XM_005262070.2:c.3471_3472delinsTG XP_005262127.1:p.Pro1157=
XM_006724616.2:c.3471_3472delinsTG XP_006724679.1:p.Pro1157=
XM_011530849.1:c.3147_3148delinsTG XP_011529151.1:p.Pro1049=
XM_011530850.1:c.3471_3472delinsTG XP_011529152.1:p.Pro1157=
XM_011530851.1:c.1044_1045delinsTG XP_011529153.1:p.Pro348=
XM_011530849.2:c.3486_3487delinsTG XP_011529151.2:p.Pro1162=
XM_017029259.2:c.3486_3487delinsTG XP_016884748.1:p.Pro1162=
XM_017029260.1:c.3486_3487delinsTG XP_016884749.1:p.Pro1162=
XM_017029261.1:c.3486_3487delinsTG XP_016884750.1:p.Pro1162=
XM_017029262.2:c.3486_3487delinsTG XP_016884751.1:p.Pro1162=
XM_017029263.2:c.1806_1807delinsTG XP_016884752.1:p.Pro602=
NM_000495.5:c.3471_3472delinsTG NP_000486.1:p.Pro1157=
NM_033380.3:c.3471_3472delinsTG MANE Select NP_203699.1:p.Pro1157=