Canonical Allele Identifier: CA2450719155
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108687364C= , CM000685.2:g.108687364C= GRCh38
NC_000023.10:g.107930594C= , CM000685.1:g.107930594C= GRCh37
NC_000023.9:g.107817250C= NCBI36
NG_011977.1:g.252441C=
NG_011977.2:g.252441C=

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.4316-118C= MANE Select ENSP00000331902.7:n.4316-118C=
ENST00000361603.7:c.4298-118C= ENSP00000354505.2:n.4298-118C=
ENST00000510690.2:n.810-118C=
ENST00000328300.10:c.4316-118C= ENSP00000331902.6:n.4316-118C=
ENST00000361603.6:c.4298-118C= ENSP00000354505.2:n.4298-118C=
ENST00000489230.1:n.719-118C=
ENST00000515658.1:c.112-118C=
NM_000495.4:c.4298-118C= NP_000486.1:n.4298-118C=
NM_033380.2:c.4316-118C= NP_203699.1:n.4316-118C=
XM_005262070.2:c.4307-118C= XP_005262127.1:n.4307-118C=
XM_006724616.2:c.4316-118C= XP_006724679.1:n.4316-118C=
XM_011530849.1:c.3992-118C= XP_011529151.1:n.3992-118C=
XM_011530851.1:c.1889-118C= XP_011529153.1:n.1889-118C=
XM_011530849.2:c.4331-118C= XP_011529151.2:n.4331-118C=
XM_017029259.2:c.4322-118C= XP_016884748.1:n.4322-118C=
XM_017029260.1:c.4313-118C= XP_016884749.1:n.4313-118C=
XM_017029263.2:c.2651-118C= XP_016884752.1:n.2651-118C=
NM_000495.5:c.4298-118C= NP_000486.1:n.4298-118C=
NM_033380.3:c.4316-118C= MANE Select NP_203699.1:n.4316-118C=