Canonical Allele Identifier: CA2450722136
Gene: COL4A5 HGNC NCBI

Linked Data

dbSNP Id: rs2068737046

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108696502T>C , CM000685.2:g.108696502T>C GRCh38
NC_000023.10:g.107939732T>C , CM000685.1:g.107939732T>C GRCh37
NC_000023.9:g.107826388T>C NCBI36
NG_011977.1:g.261579T>C
NG_011977.2:g.261579T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.*124T>C MANE Select ENSP00000331902.7:n.*124T>C
ENST00000361603.7:c.*124T>C ENSP00000354505.2:n.*124T>C
ENST00000644079.1:n.2888T>C
ENST00000328300.10:c.*124T>C ENSP00000331902.6:n.*124T>C
ENST00000361603.6:c.*124T>C ENSP00000354505.2:n.*124T>C
ENST00000504541.1:c.425T>C ENSP00000424845.1:n.425T>C
ENST00000515658.1:c.530T>C
NM_000495.4:c.*124T>C NP_000486.1:n.*124T>C
NM_033380.2:c.*124T>C NP_203699.1:n.*124T>C
XM_005262070.2:c.*124T>C XP_005262127.1:n.*124T>C
XM_006724616.2:c.*124T>C XP_006724679.1:n.*124T>C
XM_011530849.1:c.*124T>C XP_011529151.1:n.*124T>C
XM_011530851.1:c.*124T>C XP_011529153.1:n.*124T>C
XM_011530849.2:c.*124T>C XP_011529151.2:n.*124T>C
XM_017029259.2:c.*124T>C XP_016884748.1:n.*124T>C
XM_017029260.1:c.*124T>C XP_016884749.1:n.*124T>C
XM_017029263.2:c.*124T>C XP_016884752.1:n.*124T>C
NM_000495.5:c.*124T>C NP_000486.1:n.*124T>C
NM_033380.3:c.*124T>C MANE Select NP_203699.1:n.*124T>C