Canonical Allele Identifier: CA259128
Gene: COL4A5 HGNC NCBI

Linked Data

dbSNP Id: rs397515494

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108695116_108695117insT , CM000685.2:g.108695116_108695117insT GRCh38
NC_000023.10:g.107938346_107938347insT , CM000685.1:g.107938346_107938347insT GRCh37
NC_000023.9:g.107825002_107825003insT NCBI36
NG_011977.1:g.260193_260194insT
NG_011977.2:g.260193_260194insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.4822-151_4822-150insT MANE Select ENSP00000331902.7:n.4822-151_4822-150insT
ENST00000361603.7:c.4804-151_4804-150insT ENSP00000354505.2:n.4804-151_4804-150insT
ENST00000510690.2:n.1316-151_1316-150insT
ENST00000644079.1:n.1502_1503insT
ENST00000328300.10:c.4822-151_4822-150insT ENSP00000331902.6:n.4822-151_4822-150insT
ENST00000361603.6:c.4804-151_4804-150insT ENSP00000354505.2:n.4804-151_4804-150insT
ENST00000504541.1:c.219+195_219+196insT ENSP00000424845.1:n.219+195_219+196insT
ENST00000515658.1:c.325-1181_325-1180insT
NM_000495.4:c.4804-151_4804-150insT NP_000486.1:n.4804-151_4804-150insT
NM_033380.2:c.4822-151_4822-150insT NP_203699.1:n.4822-151_4822-150insT
XM_005262070.2:c.4813-151_4813-150insT XP_005262127.1:n.4813-151_4813-150insT
XM_006724616.2:c.4822-151_4822-150insT XP_006724679.1:n.4822-151_4822-150insT
XM_011530849.1:c.4498-151_4498-150insT XP_011529151.1:n.4498-151_4498-150insT
XM_011530851.1:c.2395-151_2395-150insT XP_011529153.1:n.2395-151_2395-150insT
XM_011530849.2:c.4837-151_4837-150insT XP_011529151.2:n.4837-151_4837-150insT
XM_017029259.2:c.4828-151_4828-150insT XP_016884748.1:n.4828-151_4828-150insT
XM_017029260.1:c.4819-151_4819-150insT XP_016884749.1:n.4819-151_4819-150insT
XM_017029263.2:c.3157-151_3157-150insT XP_016884752.1:n.3157-151_3157-150insT
NM_000495.5:c.4804-151_4804-150insT NP_000486.1:n.4804-151_4804-150insT
NM_033380.3:c.4822-151_4822-150insT MANE Select NP_203699.1:n.4822-151_4822-150insT