Canonical Allele Identifier: CA517925698

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938076T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694846T>C , CM000685.2:g.108694846T>C	GRCh38
NC_000023.10:g.107938076T>C , CM000685.1:g.107938076T>C	GRCh37
NC_000023.9:g.107824732T>C	NCBI36
NG_011977.1:g.259923T>C
NG_011977.2:g.259923T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4746T>C MANE Select	ENSP00000331902.7:p.Val1582=
ENST00000361603.7:c.4728T>C	ENSP00000354505.2:p.Val1576=
ENST00000510690.2:n.1240T>C
ENST00000644079.1:n.1232T>C
ENST00000328300.10:c.4746T>C	ENSP00000331902.6:p.Val1582=
ENST00000361603.6:c.4728T>C	ENSP00000354505.2:p.Val1576=
ENST00000504541.1:c.144T>C	ENSP00000424845.1:p.Val48=
ENST00000515658.1:c.325-1451T>C
NM_000495.4:c.4728T>C	NP_000486.1:p.Val1576=
NM_033380.2:c.4746T>C	NP_203699.1:p.Val1582=
XM_005262070.2:c.4737T>C	XP_005262127.1:p.Val1579=
XM_006724616.2:c.4746T>C	XP_006724679.1:p.Val1582=
XM_011530849.1:c.4422T>C	XP_011529151.1:p.Val1474=
XM_011530851.1:c.2319T>C	XP_011529153.1:p.Val773=
XM_011530849.2:c.4761T>C	XP_011529151.2:p.Val1587=
XM_017029259.2:c.4752T>C	XP_016884748.1:p.Val1584=
XM_017029260.1:c.4743T>C	XP_016884749.1:p.Val1581=
XM_017029263.2:c.3081T>C	XP_016884752.1:p.Val1027=
NM_000495.5:c.4728T>C	NP_000486.1:p.Val1576=
NM_033380.3:c.4746T>C MANE Select	NP_203699.1:p.Val1582=