Canonical Allele Identifier: CA517924553

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107930800T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687570T>C , CM000685.2:g.108687570T>C	GRCh38
NC_000023.10:g.107930800T>C , CM000685.1:g.107930800T>C	GRCh37
NC_000023.9:g.107817456T>C	NCBI36
NG_011977.1:g.252647T>C
NG_011977.2:g.252647T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4404T>C MANE Select	ENSP00000331902.7:p.Phe1468=
ENST00000361603.7:c.4386T>C	ENSP00000354505.2:p.Phe1462=
ENST00000510690.2:n.898T>C
ENST00000328300.10:c.4404T>C	ENSP00000331902.6:p.Phe1468=
ENST00000361603.6:c.4386T>C	ENSP00000354505.2:p.Phe1462=
ENST00000515658.1:c.200T>C
NM_000495.4:c.4386T>C	NP_000486.1:p.Phe1462=
NM_033380.2:c.4404T>C	NP_203699.1:p.Phe1468=
XM_005262070.2:c.4395T>C	XP_005262127.1:p.Phe1465=
XM_006724616.2:c.4404T>C	XP_006724679.1:p.Phe1468=
XM_011530849.1:c.4080T>C	XP_011529151.1:p.Phe1360=
XM_011530851.1:c.1977T>C	XP_011529153.1:p.Phe659=
XM_011530849.2:c.4419T>C	XP_011529151.2:p.Phe1473=
XM_017029259.2:c.4410T>C	XP_016884748.1:p.Phe1470=
XM_017029260.1:c.4401T>C	XP_016884749.1:p.Phe1467=
XM_017029263.2:c.2739T>C	XP_016884752.1:p.Phe913=
NM_000495.5:c.4386T>C	NP_000486.1:p.Phe1462=
NM_033380.3:c.4404T>C MANE Select	NP_203699.1:p.Phe1468=