Canonical Allele Identifier: CA2694415575
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108695157T>C , CM000685.2:g.108695157T>C GRCh38
NC_000023.10:g.107938387T>C , CM000685.1:g.107938387T>C GRCh37
NC_000023.9:g.107825043T>C NCBI36
NG_011977.1:g.260234T>C
NG_011977.2:g.260234T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.4822-110T>C MANE Select ENSP00000331902.7:n.4822-110T>C
ENST00000361603.7:c.4804-110T>C ENSP00000354505.2:n.4804-110T>C
ENST00000510690.2:n.1316-110T>C
ENST00000644079.1:n.1543T>C
ENST00000328300.10:c.4822-110T>C ENSP00000331902.6:n.4822-110T>C
ENST00000361603.6:c.4804-110T>C ENSP00000354505.2:n.4804-110T>C
ENST00000504541.1:c.219+236T>C ENSP00000424845.1:n.219+236T>C
ENST00000515658.1:c.325-1140T>C
NM_000495.4:c.4804-110T>C NP_000486.1:n.4804-110T>C
NM_033380.2:c.4822-110T>C NP_203699.1:n.4822-110T>C
XM_005262070.2:c.4813-110T>C XP_005262127.1:n.4813-110T>C
XM_006724616.2:c.4822-110T>C XP_006724679.1:n.4822-110T>C
XM_011530849.1:c.4498-110T>C XP_011529151.1:n.4498-110T>C
XM_011530851.1:c.2395-110T>C XP_011529153.1:n.2395-110T>C
XM_011530849.2:c.4837-110T>C XP_011529151.2:n.4837-110T>C
XM_017029259.2:c.4828-110T>C XP_016884748.1:n.4828-110T>C
XM_017029260.1:c.4819-110T>C XP_016884749.1:n.4819-110T>C
XM_017029263.2:c.3157-110T>C XP_016884752.1:n.3157-110T>C
NM_000495.5:c.4804-110T>C NP_000486.1:n.4804-110T>C
NM_033380.3:c.4822-110T>C MANE Select NP_203699.1:n.4822-110T>C