Canonical Allele Identifier: CA2694415530
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108695077_108695082dup , CM000685.2:g.108695077_108695082dup GRCh38
NC_000023.10:g.107938307_107938312dup , CM000685.1:g.107938307_107938312dup GRCh37
NC_000023.9:g.107824963_107824968dup NCBI36
NG_011977.1:g.260154_260159dup
NG_011977.2:g.260154_260159dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.4821+156_4821+161dup MANE Select ENSP00000331902.7:n.4821+156_4821+161dup
ENST00000361603.7:c.4803+156_4803+161dup ENSP00000354505.2:n.4803+156_4803+161dup
ENST00000510690.2:n.1315+156_1315+161dup
ENST00000644079.1:n.1463_1468dup
ENST00000328300.10:c.4821+156_4821+161dup ENSP00000331902.6:n.4821+156_4821+161dup
ENST00000361603.6:c.4803+156_4803+161dup ENSP00000354505.2:n.4803+156_4803+161dup
ENST00000504541.1:c.219+156_219+161dup ENSP00000424845.1:n.219+156_219+161dup
ENST00000515658.1:c.325-1220_325-1215dup
NM_000495.4:c.4803+156_4803+161dup NP_000486.1:n.4803+156_4803+161dup
NM_033380.2:c.4821+156_4821+161dup NP_203699.1:n.4821+156_4821+161dup
XM_005262070.2:c.4812+156_4812+161dup XP_005262127.1:n.4812+156_4812+161dup
XM_006724616.2:c.4821+156_4821+161dup XP_006724679.1:n.4821+156_4821+161dup
XM_011530849.1:c.4497+156_4497+161dup XP_011529151.1:n.4497+156_4497+161dup
XM_011530851.1:c.2394+156_2394+161dup XP_011529153.1:n.2394+156_2394+161dup
XM_011530849.2:c.4836+156_4836+161dup XP_011529151.2:n.4836+156_4836+161dup
XM_017029259.2:c.4827+156_4827+161dup XP_016884748.1:n.4827+156_4827+161dup
XM_017029260.1:c.4818+156_4818+161dup XP_016884749.1:n.4818+156_4818+161dup
XM_017029263.2:c.3156+156_3156+161dup XP_016884752.1:n.3156+156_3156+161dup
NM_000495.5:c.4803+156_4803+161dup NP_000486.1:n.4803+156_4803+161dup
NM_033380.3:c.4821+156_4821+161dup MANE Select NP_203699.1:n.4821+156_4821+161dup