Canonical Allele Identifier: CA2450684310
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108584365_108584373delinsCATTTGAGG , CM000685.2:g.108584365_108584373delinsCATTTGAGG GRCh38
NC_000023.10:g.107827595_107827603delinsCATTTGAGG , CM000685.1:g.107827595_107827603delinsCATTTGAGG GRCh37
NC_000023.9:g.107714251_107714259delinsCATTTGAGG NCBI36
NG_011977.1:g.149442_149450delinsCATTTGAGG
NG_011977.2:g.149442_149450delinsCATTTGAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.991-119_991-111delinsCATTTGAGG MANE Select ENSP00000331902.7:n.991-119_991-111delinsCATTTGAGG
ENST00000361603.7:c.991-119_991-111delinsCATTTGAGG ENSP00000354505.2:n.991-119_991-111delinsCATTTGAGG
ENST00000328300.10:c.991-119_991-111delinsCATTTGAGG ENSP00000331902.6:n.991-119_991-111delinsCATTTGAGG
ENST00000361603.6:c.991-119_991-111delinsCATTTGAGG ENSP00000354505.2:n.991-119_991-111delinsCATTTGAGG
ENST00000483338.1:n.447-119_447-111delinsCATTTGAGG
NM_000495.4:c.991-119_991-111delinsCATTTGAGG NP_000486.1:n.991-119_991-111delinsCATTTGAGG
NM_033380.2:c.991-119_991-111delinsCATTTGAGG NP_203699.1:n.991-119_991-111delinsCATTTGAGG
XM_005262070.2:c.991-119_991-111delinsCATTTGAGG XP_005262127.1:n.991-119_991-111delinsCATTTGAGG
XM_005262072.3:c.991-119_991-111delinsCATTTGAGG XP_005262129.1:n.991-119_991-111delinsCATTTGAGG
XM_006724616.2:c.991-119_991-111delinsCATTTGAGG XP_006724679.1:n.991-119_991-111delinsCATTTGAGG
XM_011530849.1:c.667-119_667-111delinsCATTTGAGG XP_011529151.1:n.667-119_667-111delinsCATTTGAGG
XM_011530850.1:c.991-119_991-111delinsCATTTGAGG XP_011529152.1:n.991-119_991-111delinsCATTTGAGG
XM_011530849.2:c.1006-119_1006-111delinsCATTTGAGG XP_011529151.2:n.1006-119_1006-111delinsCATTTGAGG
XM_017029259.2:c.1006-119_1006-111delinsCATTTGAGG XP_016884748.1:n.1006-119_1006-111delinsCATTTGAGG
XM_017029260.1:c.1006-119_1006-111delinsCATTTGAGG XP_016884749.1:n.1006-119_1006-111delinsCATTTGAGG
XM_017029261.1:c.1006-119_1006-111delinsCATTTGAGG XP_016884750.1:n.1006-119_1006-111delinsCATTTGAGG
XM_017029262.2:c.1006-119_1006-111delinsCATTTGAGG XP_016884751.1:n.1006-119_1006-111delinsCATTTGAGG
XM_017029263.2:c.-719-119_-719-111delinsCATTTGAGG XP_016884752.1:n.-719-119_-719-111delinsCATTTGAGG
NM_000495.5:c.991-119_991-111delinsCATTTGAGG NP_000486.1:n.991-119_991-111delinsCATTTGAGG
NM_033380.3:c.991-119_991-111delinsCATTTGAGG MANE Select NP_203699.1:n.991-119_991-111delinsCATTTGAGG