Canonical Allele Identifier: CA517925787

Gene: COL4A5

Linked Data

• ClinVar Variation Id: 2750481
• ClinVar RCV Id: RCV003563476
• MyVariant Identifiers: chrX:g.107938097T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694867T>C , CM000685.2:g.108694867T>C	GRCh38
NC_000023.10:g.107938097T>C , CM000685.1:g.107938097T>C	GRCh37
NC_000023.9:g.107824753T>C	NCBI36
NG_011977.1:g.259944T>C
NG_011977.2:g.259944T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4767T>C MANE Select	ENSP00000331902.7:p.Ile1589=
ENST00000361603.7:c.4749T>C	ENSP00000354505.2:p.Ile1583=
ENST00000510690.2:n.1261T>C
ENST00000644079.1:n.1253T>C
ENST00000328300.10:c.4767T>C	ENSP00000331902.6:p.Ile1589=
ENST00000361603.6:c.4749T>C	ENSP00000354505.2:p.Ile1583=
ENST00000504541.1:c.165T>C	ENSP00000424845.1:p.Ile55=
ENST00000515658.1:c.325-1430T>C
NM_000495.4:c.4749T>C	NP_000486.1:p.Ile1583=
NM_033380.2:c.4767T>C	NP_203699.1:p.Ile1589=
XM_005262070.2:c.4758T>C	XP_005262127.1:p.Ile1586=
XM_006724616.2:c.4767T>C	XP_006724679.1:p.Ile1589=
XM_011530849.1:c.4443T>C	XP_011529151.1:p.Ile1481=
XM_011530851.1:c.2340T>C	XP_011529153.1:p.Ile780=
XM_011530849.2:c.4782T>C	XP_011529151.2:p.Ile1594=
XM_017029259.2:c.4773T>C	XP_016884748.1:p.Ile1591=
XM_017029260.1:c.4764T>C	XP_016884749.1:p.Ile1588=
XM_017029263.2:c.3102T>C	XP_016884752.1:p.Ile1034=
NM_000495.5:c.4749T>C	NP_000486.1:p.Ile1583=
NM_033380.3:c.4767T>C MANE Select	NP_203699.1:p.Ile1589=