Canonical Allele Identifier: CA2450718740
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108685999T= , CM000685.2:g.108685999T= GRCh38
NC_000023.10:g.107929229T= , CM000685.1:g.107929229T= GRCh37
NC_000023.9:g.107815885T= NCBI36
NG_011977.1:g.251076T=
NG_011977.2:g.251076T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.4217-32T= MANE Select ENSP00000331902.7:n.4217-32T=
ENST00000361603.7:c.4199-32T= ENSP00000354505.2:n.4199-32T=
ENST00000510690.2:n.711-32T=
ENST00000328300.10:c.4217-32T= ENSP00000331902.6:n.4217-32T=
ENST00000361603.6:c.4199-32T= ENSP00000354505.2:n.4199-32T=
ENST00000489230.1:n.620-32T=
ENST00000515658.1:c.13-32T=
NM_000495.4:c.4199-32T= NP_000486.1:n.4199-32T=
NM_033380.2:c.4217-32T= NP_203699.1:n.4217-32T=
XM_005262070.2:c.4208-32T= XP_005262127.1:n.4208-32T=
XM_006724616.2:c.4217-32T= XP_006724679.1:n.4217-32T=
XM_011530849.1:c.3893-32T= XP_011529151.1:n.3893-32T=
XM_011530851.1:c.1790-32T= XP_011529153.1:n.1790-32T=
XM_011530849.2:c.4232-32T= XP_011529151.2:n.4232-32T=
XM_017029259.2:c.4223-32T= XP_016884748.1:n.4223-32T=
XM_017029260.1:c.4214-32T= XP_016884749.1:n.4214-32T=
XM_017029263.2:c.2552-32T= XP_016884752.1:n.2552-32T=
NM_000495.5:c.4199-32T= NP_000486.1:n.4199-32T=
NM_033380.3:c.4217-32T= MANE Select NP_203699.1:n.4217-32T=