Canonical Allele Identifier: CA2694411385
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108575843dup , CM000685.2:g.108575843dup GRCh38
NC_000023.10:g.107819073dup , CM000685.1:g.107819073dup GRCh37
NC_000023.9:g.107705729dup NCBI36
NG_011977.1:g.140920dup
NG_011977.2:g.140920dup

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.547-67dup MANE Select ENSP00000331902.7:n.547-67dup
ENST00000361603.7:c.547-67dup ENSP00000354505.2:n.547-67dup
ENST00000328300.10:c.547-67dup ENSP00000331902.6:n.547-67dup
ENST00000361603.6:c.547-67dup ENSP00000354505.2:n.547-67dup
NM_000495.4:c.547-67dup NP_000486.1:n.547-67dup
NM_033380.2:c.547-67dup NP_203699.1:n.547-67dup
XM_005262070.2:c.547-67dup XP_005262127.1:n.547-67dup
XM_005262072.3:c.547-67dup XP_005262129.1:n.547-67dup
XM_006724616.2:c.547-67dup XP_006724679.1:n.547-67dup
XM_011530849.1:c.223-67dup XP_011529151.1:n.223-67dup
XM_011530850.1:c.547-67dup XP_011529152.1:n.547-67dup
XM_011530849.2:c.562-67dup XP_011529151.2:n.562-67dup
XM_017029259.2:c.562-67dup XP_016884748.1:n.562-67dup
XM_017029260.1:c.562-67dup XP_016884749.1:n.562-67dup
XM_017029261.1:c.562-67dup XP_016884750.1:n.562-67dup
XM_017029262.2:c.562-67dup XP_016884751.1:n.562-67dup
NM_000495.5:c.547-67dup NP_000486.1:n.547-67dup
NM_033380.3:c.547-67dup MANE Select NP_203699.1:n.547-67dup