Canonical Allele Identifier: CA258914
Gene: COL4A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 24662
ClinVar RCV Id: RCV001328190
dbSNP Id: rs104886247

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108668346G>A , CM000685.2:g.108668346G>A GRCh38
NC_000023.10:g.107911576G>A , CM000685.1:g.107911576G>A GRCh37
NC_000023.9:g.107798232G>A NCBI36
NG_011977.1:g.233423G>A
NG_011977.2:g.233423G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.3632G>A MANE Select ENSP00000331902.7:p.Gly1211Glu
ENST00000361603.7:c.3632G>A ENSP00000354505.2:p.Gly1211Glu
ENST00000328300.10:c.3632G>A ENSP00000331902.6:p.Gly1211Glu
ENST00000361603.6:c.3632G>A ENSP00000354505.2:p.Gly1211Glu
NM_000495.4:c.3632G>A NP_000486.1:p.Gly1211Glu
NM_033380.2:c.3632G>A NP_203699.1:p.Gly1211Glu
XM_005262070.2:c.3632G>A XP_005262127.1:p.Gly1211Glu
XM_006724616.2:c.3632G>A XP_006724679.1:p.Gly1211Glu
XM_011530849.1:c.3308G>A XP_011529151.1:p.Gly1103Glu
XM_011530850.1:c.3632G>A XP_011529152.1:p.Gly1211Glu
XM_011530851.1:c.1205G>A XP_011529153.1:p.Gly402Glu
XM_011530849.2:c.3647G>A XP_011529151.2:p.Gly1216Glu
XM_017029259.2:c.3647G>A XP_016884748.1:p.Gly1216Glu
XM_017029260.1:c.3647G>A XP_016884749.1:p.Gly1216Glu
XM_017029261.1:c.3647G>A XP_016884750.1:p.Gly1216Glu
XM_017029262.2:c.3647G>A XP_016884751.1:p.Gly1216Glu
XM_017029263.2:c.1967G>A XP_016884752.1:p.Gly656Glu
NM_000495.5:c.3632G>A NP_000486.1:p.Gly1211Glu
NM_033380.3:c.3632G>A MANE Select NP_203699.1:p.Gly1211Glu