Canonical Allele Identifier: CA413853931

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107930718G>C (hg19) ; chrX:g.108687488G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687488G>C , CM000685.2:g.108687488G>C	GRCh38
NC_000023.10:g.107930718G>C , CM000685.1:g.107930718G>C	GRCh37
NC_000023.9:g.107817374G>C	NCBI36
NG_011977.1:g.252565G>C
NG_011977.2:g.252565G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4322G>C MANE Select	ENSP00000331902.7:p.Arg1441Pro
ENST00000361603.7:c.4304G>C	ENSP00000354505.2:p.Arg1435Pro
ENST00000510690.2:n.816G>C
ENST00000328300.10:c.4322G>C	ENSP00000331902.6:p.Arg1441Pro
ENST00000361603.6:c.4304G>C	ENSP00000354505.2:p.Arg1435Pro
ENST00000489230.1:n.725G>C
ENST00000515658.1:c.118G>C
NM_000495.4:c.4304G>C	NP_000486.1:p.Arg1435Pro
NM_033380.2:c.4322G>C	NP_203699.1:p.Arg1441Pro
XM_005262070.2:c.4313G>C	XP_005262127.1:p.Arg1438Pro
XM_006724616.2:c.4322G>C	XP_006724679.1:p.Arg1441Pro
XM_011530849.1:c.3998G>C	XP_011529151.1:p.Arg1333Pro
XM_011530851.1:c.1895G>C	XP_011529153.1:p.Arg632Pro
XM_011530849.2:c.4337G>C	XP_011529151.2:p.Arg1446Pro
XM_017029259.2:c.4328G>C	XP_016884748.1:p.Arg1443Pro
XM_017029260.1:c.4319G>C	XP_016884749.1:p.Arg1440Pro
XM_017029263.2:c.2657G>C	XP_016884752.1:p.Arg886Pro
NM_000495.5:c.4304G>C	NP_000486.1:p.Arg1435Pro
NM_033380.3:c.4322G>C MANE Select	NP_203699.1:p.Arg1441Pro