Canonical Allele Identifier: CA2450721634
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108695002C= , CM000685.2:g.108695002C= GRCh38
NC_000023.10:g.107938232C= , CM000685.1:g.107938232C= GRCh37
NC_000023.9:g.107824888C= NCBI36
NG_011977.1:g.260079C=
NG_011977.2:g.260079C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.4821+81C= MANE Select ENSP00000331902.7:n.4821+81C=
ENST00000361603.7:c.4803+81C= ENSP00000354505.2:n.4803+81C=
ENST00000510690.2:n.1315+81C=
ENST00000644079.1:n.1388C=
ENST00000328300.10:c.4821+81C= ENSP00000331902.6:n.4821+81C=
ENST00000361603.6:c.4803+81C= ENSP00000354505.2:n.4803+81C=
ENST00000504541.1:c.219+81C= ENSP00000424845.1:n.219+81C=
ENST00000515658.1:c.325-1295C=
NM_000495.4:c.4803+81C= NP_000486.1:n.4803+81C=
NM_033380.2:c.4821+81C= NP_203699.1:n.4821+81C=
XM_005262070.2:c.4812+81C= XP_005262127.1:n.4812+81C=
XM_006724616.2:c.4821+81C= XP_006724679.1:n.4821+81C=
XM_011530849.1:c.4497+81C= XP_011529151.1:n.4497+81C=
XM_011530851.1:c.2394+81C= XP_011529153.1:n.2394+81C=
XM_011530849.2:c.4836+81C= XP_011529151.2:n.4836+81C=
XM_017029259.2:c.4827+81C= XP_016884748.1:n.4827+81C=
XM_017029260.1:c.4818+81C= XP_016884749.1:n.4818+81C=
XM_017029263.2:c.3156+81C= XP_016884752.1:n.3156+81C=
NM_000495.5:c.4803+81C= NP_000486.1:n.4803+81C=
NM_033380.3:c.4821+81C= MANE Select NP_203699.1:n.4821+81C=