Canonical Allele Identifier: CA2450715756
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108677506C= , CM000685.2:g.108677506C= GRCh38
NC_000023.10:g.107920736C= , CM000685.1:g.107920736C= GRCh37
NC_000023.9:g.107807392C= NCBI36
NG_011977.1:g.242583C=
NG_011977.2:g.242583C=

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.3815C= MANE Select ENSP00000331902.7:p.Pro1272=
ENST00000361603.7:c.3797C= ENSP00000354505.2:p.Pro1266=
ENST00000510690.2:n.309C=
ENST00000328300.10:c.3815C= ENSP00000331902.6:p.Pro1272=
ENST00000361603.6:c.3797C= ENSP00000354505.2:p.Pro1266=
ENST00000489230.1:n.218C=
ENST00000510690.1:n.309C=
NM_000495.4:c.3797C= NP_000486.1:p.Pro1266=
NM_033380.2:c.3815C= NP_203699.1:p.Pro1272=
XM_005262070.2:c.3806C= XP_005262127.1:p.Pro1269=
XM_006724616.2:c.3815C= XP_006724679.1:p.Pro1272=
XM_011530849.1:c.3491C= XP_011529151.1:p.Pro1164=
XM_011530851.1:c.1388C= XP_011529153.1:p.Pro463=
XM_011530849.2:c.3830C= XP_011529151.2:p.Pro1277=
XM_017029259.2:c.3821C= XP_016884748.1:p.Pro1274=
XM_017029260.1:c.3812C= XP_016884749.1:p.Pro1271=
XM_017029261.1:c.3830C= XP_016884750.1:p.Pro1277=
XM_017029263.2:c.2150C= XP_016884752.1:p.Pro717=
NM_000495.5:c.3797C= NP_000486.1:p.Pro1266=
NM_033380.3:c.3815C= MANE Select NP_203699.1:p.Pro1272=