Canonical Allele Identifier: CA414132462

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938077C>A (hg19) ; chrX:g.108694847C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694847C>A , CM000685.2:g.108694847C>A	GRCh38
NC_000023.10:g.107938077C>A , CM000685.1:g.107938077C>A	GRCh37
NC_000023.9:g.107824733C>A	NCBI36
NG_011977.1:g.259924C>A
NG_011977.2:g.259924C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4747C>A MANE Select	ENSP00000331902.7:p.His1583Asn
ENST00000361603.7:c.4729C>A	ENSP00000354505.2:p.His1577Asn
ENST00000510690.2:n.1241C>A
ENST00000644079.1:n.1233C>A
ENST00000328300.10:c.4747C>A	ENSP00000331902.6:p.His1583Asn
ENST00000361603.6:c.4729C>A	ENSP00000354505.2:p.His1577Asn
ENST00000504541.1:c.145C>A	ENSP00000424845.1:p.His49Asn
ENST00000515658.1:c.325-1450C>A
NM_000495.4:c.4729C>A	NP_000486.1:p.His1577Asn
NM_033380.2:c.4747C>A	NP_203699.1:p.His1583Asn
XM_005262070.2:c.4738C>A	XP_005262127.1:p.His1580Asn
XM_006724616.2:c.4747C>A	XP_006724679.1:p.His1583Asn
XM_011530849.1:c.4423C>A	XP_011529151.1:p.His1475Asn
XM_011530851.1:c.2320C>A	XP_011529153.1:p.His774Asn
XM_011530849.2:c.4762C>A	XP_011529151.2:p.His1588Asn
XM_017029259.2:c.4753C>A	XP_016884748.1:p.His1585Asn
XM_017029260.1:c.4744C>A	XP_016884749.1:p.His1582Asn
XM_017029263.2:c.3082C>A	XP_016884752.1:p.His1028Asn
NM_000495.5:c.4729C>A	NP_000486.1:p.His1577Asn
NM_033380.3:c.4747C>A MANE Select	NP_203699.1:p.His1583Asn