Canonical Allele Identifier: CA517925957

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938136T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694906T>G , CM000685.2:g.108694906T>G	GRCh38
NC_000023.10:g.107938136T>G , CM000685.1:g.107938136T>G	GRCh37
NC_000023.9:g.107824792T>G	NCBI36
NG_011977.1:g.259983T>G
NG_011977.2:g.259983T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4806T>G MANE Select	ENSP00000331902.7:p.Gly1602=
ENST00000361603.7:c.4788T>G	ENSP00000354505.2:p.Gly1596=
ENST00000510690.2:n.1300T>G
ENST00000644079.1:n.1292T>G
ENST00000328300.10:c.4806T>G	ENSP00000331902.6:p.Gly1602=
ENST00000361603.6:c.4788T>G	ENSP00000354505.2:p.Gly1596=
ENST00000504541.1:c.204T>G	ENSP00000424845.1:p.Gly68=
ENST00000515658.1:c.325-1391T>G
NM_000495.4:c.4788T>G	NP_000486.1:p.Gly1596=
NM_033380.2:c.4806T>G	NP_203699.1:p.Gly1602=
XM_005262070.2:c.4797T>G	XP_005262127.1:p.Gly1599=
XM_006724616.2:c.4806T>G	XP_006724679.1:p.Gly1602=
XM_011530849.1:c.4482T>G	XP_011529151.1:p.Gly1494=
XM_011530851.1:c.2379T>G	XP_011529153.1:p.Gly793=
XM_011530849.2:c.4821T>G	XP_011529151.2:p.Gly1607=
XM_017029259.2:c.4812T>G	XP_016884748.1:p.Gly1604=
XM_017029260.1:c.4803T>G	XP_016884749.1:p.Gly1601=
XM_017029263.2:c.3141T>G	XP_016884752.1:p.Gly1047=
NM_000495.5:c.4788T>G	NP_000486.1:p.Gly1596=
NM_033380.3:c.4806T>G MANE Select	NP_203699.1:p.Gly1602=