Canonical Allele Identifier: CA414132652
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108695273A>T , CM000685.2:g.108695273A>T GRCh38
NC_000023.10:g.107938503A>T , CM000685.1:g.107938503A>T GRCh37
NC_000023.9:g.107825159A>T NCBI36
NG_011977.1:g.260350A>T
NG_011977.2:g.260350A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.4828A>T MANE Select ENSP00000331902.7:p.Ser1610Cys
ENST00000361603.7:c.4810A>T ENSP00000354505.2:p.Ser1604Cys
ENST00000510690.2:n.1322A>T
ENST00000644079.1:n.1659A>T
ENST00000328300.10:c.4828A>T ENSP00000331902.6:p.Ser1610Cys
ENST00000361603.6:c.4810A>T ENSP00000354505.2:p.Ser1604Cys
ENST00000504541.1:c.219+352A>T ENSP00000424845.1:n.219+352A>T
ENST00000515658.1:c.325-1024A>T
NM_000495.4:c.4810A>T NP_000486.1:p.Ser1604Cys
NM_033380.2:c.4828A>T NP_203699.1:p.Ser1610Cys
XM_005262070.2:c.4819A>T XP_005262127.1:p.Ser1607Cys
XM_006724616.2:c.4828A>T XP_006724679.1:p.Ser1610Cys
XM_011530849.1:c.4504A>T XP_011529151.1:p.Ser1502Cys
XM_011530851.1:c.2401A>T XP_011529153.1:p.Ser801Cys
XM_011530849.2:c.4843A>T XP_011529151.2:p.Ser1615Cys
XM_017029259.2:c.4834A>T XP_016884748.1:p.Ser1612Cys
XM_017029260.1:c.4825A>T XP_016884749.1:p.Ser1609Cys
XM_017029263.2:c.3163A>T XP_016884752.1:p.Ser1055Cys
NM_000495.5:c.4810A>T NP_000486.1:p.Ser1604Cys
NM_033380.3:c.4828A>T MANE Select NP_203699.1:p.Ser1610Cys