Canonical Allele Identifier: CA517922749

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107911709G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108668479G>A , CM000685.2:g.108668479G>A	GRCh38
NC_000023.10:g.107911709G>A , CM000685.1:g.107911709G>A	GRCh37
NC_000023.9:g.107798365G>A	NCBI36
NG_011977.1:g.233556G>A
NG_011977.2:g.233556G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.3765G>A MANE Select	ENSP00000331902.7:p.Gly1255=
ENST00000361603.7:c.3765G>A	ENSP00000354505.2:p.Gly1255=
ENST00000328300.10:c.3765G>A	ENSP00000331902.6:p.Gly1255=
ENST00000361603.6:c.3765G>A	ENSP00000354505.2:p.Gly1255=
NM_000495.4:c.3765G>A	NP_000486.1:p.Gly1255=
NM_033380.2:c.3765G>A	NP_203699.1:p.Gly1255=
XM_005262070.2:c.3765G>A	XP_005262127.1:p.Gly1255=
XM_006724616.2:c.3765G>A	XP_006724679.1:p.Gly1255=
XM_011530849.1:c.3441G>A	XP_011529151.1:p.Gly1147=
XM_011530850.1:c.3765G>A	XP_011529152.1:p.Gly1255=
XM_011530851.1:c.1338G>A	XP_011529153.1:p.Gly446=
XM_011530849.2:c.3780G>A	XP_011529151.2:p.Gly1260=
XM_017029259.2:c.3780G>A	XP_016884748.1:p.Gly1260=
XM_017029260.1:c.3780G>A	XP_016884749.1:p.Gly1260=
XM_017029261.1:c.3780G>A	XP_016884750.1:p.Gly1260=
XM_017029262.2:c.3780G>A	XP_016884751.1:p.Gly1260=
XM_017029263.2:c.2100G>A	XP_016884752.1:p.Gly700=
NM_000495.5:c.3765G>A	NP_000486.1:p.Gly1255=
NM_033380.3:c.3765G>A MANE Select	NP_203699.1:p.Gly1255=