Canonical Allele Identifier: CA517926124

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938596A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695366A>C , CM000685.2:g.108695366A>C	GRCh38
NC_000023.10:g.107938596A>C , CM000685.1:g.107938596A>C	GRCh37
NC_000023.9:g.107825252A>C	NCBI36
NG_011977.1:g.260443A>C
NG_011977.2:g.260443A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4921A>C MANE Select	ENSP00000331902.7:p.Arg1641=
ENST00000361603.7:c.4903A>C	ENSP00000354505.2:p.Arg1635=
ENST00000510690.2:n.1415A>C
ENST00000644079.1:n.1752A>C
ENST00000328300.10:c.4921A>C	ENSP00000331902.6:p.Arg1641=
ENST00000361603.6:c.4903A>C	ENSP00000354505.2:p.Arg1635=
ENST00000504541.1:c.219+445A>C	ENSP00000424845.1:n.219+445A>C
ENST00000515658.1:c.325-931A>C
NM_000495.4:c.4903A>C	NP_000486.1:p.Arg1635=
NM_033380.2:c.4921A>C	NP_203699.1:p.Arg1641=
XM_005262070.2:c.4912A>C	XP_005262127.1:p.Arg1638=
XM_006724616.2:c.4921A>C	XP_006724679.1:p.Arg1641=
XM_011530849.1:c.4597A>C	XP_011529151.1:p.Arg1533=
XM_011530851.1:c.2494A>C	XP_011529153.1:p.Arg832=
XM_011530849.2:c.4936A>C	XP_011529151.2:p.Arg1646=
XM_017029259.2:c.4927A>C	XP_016884748.1:p.Arg1643=
XM_017029260.1:c.4918A>C	XP_016884749.1:p.Arg1640=
XM_017029263.2:c.3256A>C	XP_016884752.1:p.Arg1086=
NM_000495.5:c.4903A>C	NP_000486.1:p.Arg1635=
NM_033380.3:c.4921A>C MANE Select	NP_203699.1:p.Arg1641=