Canonical Allele Identifier: CA517991651

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107816881A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108573651A>C , CM000685.2:g.108573651A>C	GRCh38
NC_000023.10:g.107816881A>C , CM000685.1:g.107816881A>C	GRCh37
NC_000023.9:g.107703537A>C	NCBI36
NG_011977.1:g.138728A>C
NG_011977.2:g.138728A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.543A>C MANE Select	ENSP00000331902.7:p.Ile181=
ENST00000361603.7:c.543A>C	ENSP00000354505.2:p.Ile181=
ENST00000328300.10:c.543A>C	ENSP00000331902.6:p.Ile181=
ENST00000361603.6:c.543A>C	ENSP00000354505.2:p.Ile181=
NM_000495.4:c.543A>C	NP_000486.1:p.Ile181=
NM_033380.2:c.543A>C	NP_203699.1:p.Ile181=
XM_005262070.2:c.543A>C	XP_005262127.1:p.Ile181=
XM_005262072.3:c.543A>C	XP_005262129.1:p.Ile181=
XM_006724616.2:c.543A>C	XP_006724679.1:p.Ile181=
XM_011530849.1:c.219A>C	XP_011529151.1:p.Ile73=
XM_011530850.1:c.543A>C	XP_011529152.1:p.Ile181=
XM_011530849.2:c.558A>C	XP_011529151.2:p.Ile186=
XM_017029259.2:c.558A>C	XP_016884748.1:p.Ile186=
XM_017029260.1:c.558A>C	XP_016884749.1:p.Ile186=
XM_017029261.1:c.558A>C	XP_016884750.1:p.Ile186=
XM_017029262.2:c.558A>C	XP_016884751.1:p.Ile186=
NM_000495.5:c.543A>C	NP_000486.1:p.Ile181=
NM_033380.3:c.543A>C MANE Select	NP_203699.1:p.Ile181=