Canonical Allele Identifier: CA2694438436
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108440270_108440271dup , CM000685.2:g.108440270_108440271dup GRCh38
NC_000023.10:g.107683500_107683501dup , CM000685.1:g.107683500_107683501dup GRCh37
NC_000023.9:g.107570156_107570157dup NCBI36
NG_011977.1:g.5347_5348dup
NG_012059.2:g.4210_4211dup
NG_011977.2:g.5347_5348dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.81+64_81+65dup MANE Select ENSP00000331902.7:n.81+64_81+65dup
ENST00000361603.7:c.81+64_81+65dup ENSP00000354505.2:n.81+64_81+65dup
ENST00000642185.1:c.81+64_81+65dup ENSP00000495101.1:n.81+64_81+65dup
ENST00000328300.10:c.81+64_81+65dup ENSP00000331902.6:n.81+64_81+65dup
ENST00000361603.6:c.81+64_81+65dup ENSP00000354505.2:n.81+64_81+65dup
ENST00000470339.1:n.265+64_265+65dup
ENST00000477429.1:n.363+64_363+65dup
NM_000495.4:c.81+64_81+65dup NP_000486.1:n.81+64_81+65dup
NM_033380.2:c.81+64_81+65dup NP_203699.1:n.81+64_81+65dup
XM_005262070.2:c.81+64_81+65dup XP_005262127.1:n.81+64_81+65dup
XM_005262072.3:c.81+64_81+65dup XP_005262129.1:n.81+64_81+65dup
XM_006724616.2:c.81+64_81+65dup XP_006724679.1:n.81+64_81+65dup
XM_011530850.1:c.81+64_81+65dup XP_011529152.1:n.81+64_81+65dup
NM_000495.5:c.81+64_81+65dup NP_000486.1:n.81+64_81+65dup
NM_033380.3:c.81+64_81+65dup MANE Select NP_203699.1:n.81+64_81+65dup