Canonical Allele Identifier: CA2450688326
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108597329_108597331delinsCTT , CM000685.2:g.108597329_108597331delinsCTT GRCh38
NC_000023.10:g.107840559_107840561delinsCTT , CM000685.1:g.107840559_107840561delinsCTT GRCh37
NC_000023.9:g.107727215_107727217delinsCTT NCBI36
NG_011977.1:g.162406_162408delinsCTT
NG_011977.2:g.162406_162408delinsCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.1588-48_1588-46delinsCTT MANE Select ENSP00000331902.7:n.1588-48_1588-46delins...
ENST00000361603.7:c.1588-48_1588-46delinsCTT ENSP00000354505.2:n.1588-48_1588-46delins...
ENST00000328300.10:c.1588-48_1588-46delinsCTT ENSP00000331902.6:n.1588-48_1588-46delins...
ENST00000361603.6:c.1588-48_1588-46delinsCTT ENSP00000354505.2:n.1588-48_1588-46delins...
ENST00000483338.1:n.1044-48_1044-46delinsCTT
NM_000495.4:c.1588-48_1588-46delinsCTT NP_000486.1:n.1588-48_1588-46delinsCTT
NM_033380.2:c.1588-48_1588-46delinsCTT NP_203699.1:n.1588-48_1588-46delinsCTT
XM_005262070.2:c.1588-48_1588-46delinsCTT XP_005262127.1:n.1588-48_1588-46delinsCTT...
XM_005262072.3:c.1588-48_1588-46delinsCTT XP_005262129.1:n.1588-48_1588-46delinsCTT...
XM_006724616.2:c.1588-48_1588-46delinsCTT XP_006724679.1:n.1588-48_1588-46delinsCTT...
XM_011530849.1:c.1264-48_1264-46delinsCTT XP_011529151.1:n.1264-48_1264-46delinsCTT...
XM_011530850.1:c.1588-48_1588-46delinsCTT XP_011529152.1:n.1588-48_1588-46delinsCTT...
XM_011530849.2:c.1603-48_1603-46delinsCTT XP_011529151.2:n.1603-48_1603-46delinsCTT...
XM_017029259.2:c.1603-48_1603-46delinsCTT XP_016884748.1:n.1603-48_1603-46delinsCTT...
XM_017029260.1:c.1603-48_1603-46delinsCTT XP_016884749.1:n.1603-48_1603-46delinsCTT...
XM_017029261.1:c.1603-48_1603-46delinsCTT XP_016884750.1:n.1603-48_1603-46delinsCTT...
XM_017029262.2:c.1603-48_1603-46delinsCTT XP_016884751.1:n.1603-48_1603-46delinsCTT...
XM_017029263.2:c.-78-48_-78-46delinsCTT XP_016884752.1:n.-78-48_-78-46delinsCTT
NM_000495.5:c.1588-48_1588-46delinsCTT NP_000486.1:n.1588-48_1588-46delinsCTT
NM_033380.3:c.1588-48_1588-46delinsCTT MANE Select NP_203699.1:n.1588-48_1588-46delinsCTT