Canonical Allele Identifier: CA414132522

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938103T>G (hg19) ; chrX:g.108694873T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694873T>G , CM000685.2:g.108694873T>G	GRCh38
NC_000023.10:g.107938103T>G , CM000685.1:g.107938103T>G	GRCh37
NC_000023.9:g.107824759T>G	NCBI36
NG_011977.1:g.259950T>G
NG_011977.2:g.259950T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4773T>G MANE Select	ENSP00000331902.7:p.His1591Gln
ENST00000361603.7:c.4755T>G	ENSP00000354505.2:p.His1585Gln
ENST00000510690.2:n.1267T>G
ENST00000644079.1:n.1259T>G
ENST00000328300.10:c.4773T>G	ENSP00000331902.6:p.His1591Gln
ENST00000361603.6:c.4755T>G	ENSP00000354505.2:p.His1585Gln
ENST00000504541.1:c.171T>G	ENSP00000424845.1:p.His57Gln
ENST00000515658.1:c.325-1424T>G
NM_000495.4:c.4755T>G	NP_000486.1:p.His1585Gln
NM_033380.2:c.4773T>G	NP_203699.1:p.His1591Gln
XM_005262070.2:c.4764T>G	XP_005262127.1:p.His1588Gln
XM_006724616.2:c.4773T>G	XP_006724679.1:p.His1591Gln
XM_011530849.1:c.4449T>G	XP_011529151.1:p.His1483Gln
XM_011530851.1:c.2346T>G	XP_011529153.1:p.His782Gln
XM_011530849.2:c.4788T>G	XP_011529151.2:p.His1596Gln
XM_017029259.2:c.4779T>G	XP_016884748.1:p.His1593Gln
XM_017029260.1:c.4770T>G	XP_016884749.1:p.His1590Gln
XM_017029263.2:c.3108T>G	XP_016884752.1:p.His1036Gln
NM_000495.5:c.4755T>G	NP_000486.1:p.His1585Gln
NM_033380.3:c.4773T>G MANE Select	NP_203699.1:p.His1591Gln