Canonical Allele Identifier: CA258539

Gene: COL4A5

Linked Data

• dbSNP Id: rs281874678
• MyVariant Identifiers: chrX:g.107840776_107840789del (hg19) ; chrX:g.108597546_108597559del (hg38)
• PubMed: PMID:20378821

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108597546_108597559del , CM000685.2:g.108597546_108597559del	GRCh38
NC_000023.10:g.107840776_107840789del , CM000685.1:g.107840776_107840789del	GRCh37
NC_000023.9:g.107727432_107727445del	NCBI36
NG_011977.1:g.162623_162636del
NG_011977.2:g.162623_162636del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.1757_1770del MANE Select	ENSP00000331902.7:p.Leu586ArgfsTer9
ENST00000361603.7:c.1757_1770del	ENSP00000354505.2:p.Leu586ArgfsTer9
ENST00000328300.10:c.1757_1770del	ENSP00000331902.6:p.Leu586ArgfsTer9
ENST00000361603.6:c.1757_1770del	ENSP00000354505.2:p.Leu586ArgfsTer9
ENST00000483338.1:n.1213_1226del
NM_000495.4:c.1757_1770del	NP_000486.1:p.Leu586ArgfsTer9
NM_033380.2:c.1757_1770del	NP_203699.1:p.Leu586ArgfsTer9
XM_005262070.2:c.1757_1770del	XP_005262127.1:p.Leu586ArgfsTer9
XM_005262072.3:c.1757_1770del	XP_005262129.1:p.Leu586ArgfsTer9
XM_006724616.2:c.1757_1770del	XP_006724679.1:p.Leu586ArgfsTer9
XM_011530849.1:c.1433_1446del	XP_011529151.1:p.Leu478ArgfsTer9
XM_011530850.1:c.1757_1770del	XP_011529152.1:p.Leu586ArgfsTer9
XM_011530849.2:c.1772_1785del	XP_011529151.2:p.Leu591ArgfsTer9
XM_017029259.2:c.1772_1785del	XP_016884748.1:p.Leu591ArgfsTer9
XM_017029260.1:c.1772_1785del	XP_016884749.1:p.Leu591ArgfsTer9
XM_017029261.1:c.1772_1785del	XP_016884750.1:p.Leu591ArgfsTer9
XM_017029262.2:c.1772_1785del	XP_016884751.1:p.Leu591ArgfsTer9
XM_017029263.2:c.92_105del	XP_016884752.1:p.Leu31ArgfsTer9
NM_000495.5:c.1757_1770del	NP_000486.1:p.Leu586ArgfsTer9
NM_033380.3:c.1757_1770del MANE Select	NP_203699.1:p.Leu586ArgfsTer9