Canonical Allele Identifier: CA2694438433
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108440263_108440264insA , CM000685.2:g.108440263_108440264insA GRCh38
NC_000023.10:g.107683493_107683494insA , CM000685.1:g.107683493_107683494insA GRCh37
NC_000023.9:g.107570149_107570150insA NCBI36
NG_011977.1:g.5340_5341insA
NG_012059.2:g.4211_4212insT
NG_011977.2:g.5340_5341insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.81+57_81+58insA MANE Select ENSP00000331902.7:n.81+57_81+58insA
ENST00000361603.7:c.81+57_81+58insA ENSP00000354505.2:n.81+57_81+58insA
ENST00000642185.1:c.81+57_81+58insA ENSP00000495101.1:n.81+57_81+58insA
ENST00000328300.10:c.81+57_81+58insA ENSP00000331902.6:n.81+57_81+58insA
ENST00000361603.6:c.81+57_81+58insA ENSP00000354505.2:n.81+57_81+58insA
ENST00000470339.1:n.265+57_265+58insA
ENST00000477429.1:n.363+57_363+58insA
NM_000495.4:c.81+57_81+58insA NP_000486.1:n.81+57_81+58insA
NM_033380.2:c.81+57_81+58insA NP_203699.1:n.81+57_81+58insA
XM_005262070.2:c.81+57_81+58insA XP_005262127.1:n.81+57_81+58insA
XM_005262072.3:c.81+57_81+58insA XP_005262129.1:n.81+57_81+58insA
XM_006724616.2:c.81+57_81+58insA XP_006724679.1:n.81+57_81+58insA
XM_011530850.1:c.81+57_81+58insA XP_011529152.1:n.81+57_81+58insA
NM_000495.5:c.81+57_81+58insA NP_000486.1:n.81+57_81+58insA
NM_033380.3:c.81+57_81+58insA MANE Select NP_203699.1:n.81+57_81+58insA