Canonical Allele Identifier: CA2450721600
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108694886T= , CM000685.2:g.108694886T= GRCh38
NC_000023.10:g.107938116T= , CM000685.1:g.107938116T= GRCh37
NC_000023.9:g.107824772T= NCBI36
NG_011977.1:g.259963T=
NG_011977.2:g.259963T=

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.4786T= MANE Select ENSP00000331902.7:p.Trp1596=
ENST00000361603.7:c.4768T= ENSP00000354505.2:p.Trp1590=
ENST00000510690.2:n.1280T=
ENST00000644079.1:n.1272T=
ENST00000328300.10:c.4786T= ENSP00000331902.6:p.Trp1596=
ENST00000361603.6:c.4768T= ENSP00000354505.2:p.Trp1590=
ENST00000504541.1:c.184T= ENSP00000424845.1:p.Trp62=
ENST00000515658.1:c.325-1411T=
NM_000495.4:c.4768T= NP_000486.1:p.Trp1590=
NM_033380.2:c.4786T= NP_203699.1:p.Trp1596=
XM_005262070.2:c.4777T= XP_005262127.1:p.Trp1593=
XM_006724616.2:c.4786T= XP_006724679.1:p.Trp1596=
XM_011530849.1:c.4462T= XP_011529151.1:p.Trp1488=
XM_011530851.1:c.2359T= XP_011529153.1:p.Trp787=
XM_011530849.2:c.4801T= XP_011529151.2:p.Trp1601=
XM_017029259.2:c.4792T= XP_016884748.1:p.Trp1598=
XM_017029260.1:c.4783T= XP_016884749.1:p.Trp1595=
XM_017029263.2:c.3121T= XP_016884752.1:p.Trp1041=
NM_000495.5:c.4768T= NP_000486.1:p.Trp1590=
NM_033380.3:c.4786T= MANE Select NP_203699.1:p.Trp1596=