Canonical Allele Identifier: CA2450719140
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108687318_108687322delinsTTTTA , CM000685.2:g.108687318_108687322delinsTTTTA GRCh38
NC_000023.10:g.107930548_107930552delinsTTTTA , CM000685.1:g.107930548_107930552delinsTTTTA GRCh37
NC_000023.9:g.107817204_107817208delinsTTTTA NCBI36
NG_011977.1:g.252395_252399delinsTTTTA
NG_011977.2:g.252395_252399delinsTTTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.4316-164_4316-160delinsTTTTA MANE Select ENSP00000331902.7:n.4316-164_4316-160delinsTTTTA
ENST00000361603.7:c.4298-164_4298-160delinsTTTTA ENSP00000354505.2:n.4298-164_4298-160delinsTTTTA
ENST00000510690.2:n.810-164_810-160delinsTTTTA
ENST00000328300.10:c.4316-164_4316-160delinsTTTTA ENSP00000331902.6:n.4316-164_4316-160delinsTTTTA
ENST00000361603.6:c.4298-164_4298-160delinsTTTTA ENSP00000354505.2:n.4298-164_4298-160delinsTTTTA
ENST00000489230.1:n.719-164_719-160delinsTTTTA
ENST00000515658.1:c.112-164_112-160delinsTTTTA
NM_000495.4:c.4298-164_4298-160delinsTTTTA NP_000486.1:n.4298-164_4298-160delinsTTTTA
NM_033380.2:c.4316-164_4316-160delinsTTTTA NP_203699.1:n.4316-164_4316-160delinsTTTTA
XM_005262070.2:c.4307-164_4307-160delinsTTTTA XP_005262127.1:n.4307-164_4307-160delinsTTTTA
XM_006724616.2:c.4316-164_4316-160delinsTTTTA XP_006724679.1:n.4316-164_4316-160delinsTTTTA
XM_011530849.1:c.3992-164_3992-160delinsTTTTA XP_011529151.1:n.3992-164_3992-160delinsTTTTA
XM_011530851.1:c.1889-164_1889-160delinsTTTTA XP_011529153.1:n.1889-164_1889-160delinsTTTTA
XM_011530849.2:c.4331-164_4331-160delinsTTTTA XP_011529151.2:n.4331-164_4331-160delinsTTTTA
XM_017029259.2:c.4322-164_4322-160delinsTTTTA XP_016884748.1:n.4322-164_4322-160delinsTTTTA
XM_017029260.1:c.4313-164_4313-160delinsTTTTA XP_016884749.1:n.4313-164_4313-160delinsTTTTA
XM_017029263.2:c.2651-164_2651-160delinsTTTTA XP_016884752.1:n.2651-164_2651-160delinsTTTTA
NM_000495.5:c.4298-164_4298-160delinsTTTTA NP_000486.1:n.4298-164_4298-160delinsTTTTA
NM_033380.3:c.4316-164_4316-160delinsTTTTA MANE Select NP_203699.1:n.4316-164_4316-160delinsTTTTA