Canonical Allele Identifier: CA413851936

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107865054T>G (hg19) ; chrX:g.108621824T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108621824T>G , CM000685.2:g.108621824T>G	GRCh38
NC_000023.10:g.107865054T>G , CM000685.1:g.107865054T>G	GRCh37
NC_000023.9:g.107751710T>G	NCBI36
NG_011977.1:g.186901T>G
NG_011977.2:g.186901T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.2699T>G MANE Select	ENSP00000331902.7:p.Met900Arg
ENST00000361603.7:c.2699T>G	ENSP00000354505.2:p.Met900Arg
ENST00000328300.10:c.2699T>G	ENSP00000331902.6:p.Met900Arg
ENST00000361603.6:c.2699T>G	ENSP00000354505.2:p.Met900Arg
ENST00000483338.1:n.2155T>G
NM_000495.4:c.2699T>G	NP_000486.1:p.Met900Arg
NM_033380.2:c.2699T>G	NP_203699.1:p.Met900Arg
XM_005262070.2:c.2699T>G	XP_005262127.1:p.Met900Arg
XM_005262072.3:c.2699T>G	XP_005262129.1:p.Met900Arg
XM_006724616.2:c.2699T>G	XP_006724679.1:p.Met900Arg
XM_011530849.1:c.2375T>G	XP_011529151.1:p.Met792Arg
XM_011530850.1:c.2699T>G	XP_011529152.1:p.Met900Arg
XM_011530851.1:c.272T>G	XP_011529153.1:p.Met91Arg
XM_011530849.2:c.2714T>G	XP_011529151.2:p.Met905Arg
XM_017029259.2:c.2714T>G	XP_016884748.1:p.Met905Arg
XM_017029260.1:c.2714T>G	XP_016884749.1:p.Met905Arg
XM_017029261.1:c.2714T>G	XP_016884750.1:p.Met905Arg
XM_017029262.2:c.2714T>G	XP_016884751.1:p.Met905Arg
XM_017029263.2:c.1034T>G	XP_016884752.1:p.Met345Arg
NM_000495.5:c.2699T>G	NP_000486.1:p.Met900Arg
NM_033380.3:c.2699T>G MANE Select	NP_203699.1:p.Met900Arg