Canonical Allele Identifier: CA2450715739
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108677461A= , CM000685.2:g.108677461A= GRCh38
NC_000023.10:g.107920691A= , CM000685.1:g.107920691A= GRCh37
NC_000023.9:g.107807347A= NCBI36
NG_011977.1:g.242538A=
NG_011977.2:g.242538A=

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.3809-39A= MANE Select ENSP00000331902.7:n.3809-39A=
ENST00000361603.7:c.3791-39A= ENSP00000354505.2:n.3791-39A=
ENST00000510690.2:n.303-39A=
ENST00000328300.10:c.3809-39A= ENSP00000331902.6:n.3809-39A=
ENST00000361603.6:c.3791-39A= ENSP00000354505.2:n.3791-39A=
ENST00000489230.1:n.212-39A=
ENST00000510690.1:n.303-39A=
NM_000495.4:c.3791-39A= NP_000486.1:n.3791-39A=
NM_033380.2:c.3809-39A= NP_203699.1:n.3809-39A=
XM_005262070.2:c.3800-39A= XP_005262127.1:n.3800-39A=
XM_006724616.2:c.3809-39A= XP_006724679.1:n.3809-39A=
XM_011530849.1:c.3485-39A= XP_011529151.1:n.3485-39A=
XM_011530851.1:c.1382-39A= XP_011529153.1:n.1382-39A=
XM_011530849.2:c.3824-39A= XP_011529151.2:n.3824-39A=
XM_017029259.2:c.3815-39A= XP_016884748.1:n.3815-39A=
XM_017029260.1:c.3806-39A= XP_016884749.1:n.3806-39A=
XM_017029261.1:c.3824-39A= XP_016884750.1:n.3824-39A=
XM_017029263.2:c.2144-39A= XP_016884752.1:n.2144-39A=
NM_000495.5:c.3791-39A= NP_000486.1:n.3791-39A=
NM_033380.3:c.3809-39A= MANE Select NP_203699.1:n.3809-39A=