Canonical Allele Identifier: CA2450721724
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108695274G= , CM000685.2:g.108695274G= GRCh38
NC_000023.10:g.107938504G= , CM000685.1:g.107938504G= GRCh37
NC_000023.9:g.107825160G= NCBI36
NG_011977.1:g.260351G=
NG_011977.2:g.260351G=

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.4829G= MANE Select ENSP00000331902.7:p.Ser1610=
ENST00000361603.7:c.4811G= ENSP00000354505.2:p.Ser1604=
ENST00000510690.2:n.1323G=
ENST00000644079.1:n.1660G=
ENST00000328300.10:c.4829G= ENSP00000331902.6:p.Ser1610=
ENST00000361603.6:c.4811G= ENSP00000354505.2:p.Ser1604=
ENST00000504541.1:c.219+353G= ENSP00000424845.1:n.219+353G=
ENST00000515658.1:c.325-1023G=
NM_000495.4:c.4811G= NP_000486.1:p.Ser1604=
NM_033380.2:c.4829G= NP_203699.1:p.Ser1610=
XM_005262070.2:c.4820G= XP_005262127.1:p.Ser1607=
XM_006724616.2:c.4829G= XP_006724679.1:p.Ser1610=
XM_011530849.1:c.4505G= XP_011529151.1:p.Ser1502=
XM_011530851.1:c.2402G= XP_011529153.1:p.Ser801=
XM_011530849.2:c.4844G= XP_011529151.2:p.Ser1615=
XM_017029259.2:c.4835G= XP_016884748.1:p.Ser1612=
XM_017029260.1:c.4826G= XP_016884749.1:p.Ser1609=
XM_017029263.2:c.3164G= XP_016884752.1:p.Ser1055=
NM_000495.5:c.4811G= NP_000486.1:p.Ser1604=
NM_033380.3:c.4829G= MANE Select NP_203699.1:p.Ser1610=