Canonical Allele Identifier: CA2450681496
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108575952C= , CM000685.2:g.108575952C= GRCh38
NC_000023.10:g.107819182C= , CM000685.1:g.107819182C= GRCh37
NC_000023.9:g.107705838C= NCBI36
NG_011977.1:g.141029C=
NG_011977.2:g.141029C=

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.589C= MANE Select ENSP00000331902.7:p.Pro197=
ENST00000361603.7:c.589C= ENSP00000354505.2:p.Pro197=
ENST00000328300.10:c.589C= ENSP00000331902.6:p.Pro197=
ENST00000361603.6:c.589C= ENSP00000354505.2:p.Pro197=
NM_000495.4:c.589C= NP_000486.1:p.Pro197=
NM_033380.2:c.589C= NP_203699.1:p.Pro197=
XM_005262070.2:c.589C= XP_005262127.1:p.Pro197=
XM_005262072.3:c.589C= XP_005262129.1:p.Pro197=
XM_006724616.2:c.589C= XP_006724679.1:p.Pro197=
XM_011530849.1:c.265C= XP_011529151.1:p.Pro89=
XM_011530850.1:c.589C= XP_011529152.1:p.Pro197=
XM_011530849.2:c.604C= XP_011529151.2:p.Pro202=
XM_017029259.2:c.604C= XP_016884748.1:p.Pro202=
XM_017029260.1:c.604C= XP_016884749.1:p.Pro202=
XM_017029261.1:c.604C= XP_016884750.1:p.Pro202=
XM_017029262.2:c.604C= XP_016884751.1:p.Pro202=
NM_000495.5:c.589C= NP_000486.1:p.Pro197=
NM_033380.3:c.589C= MANE Select NP_203699.1:p.Pro197=