Canonical Allele Identifier: CA414133190

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107939602G>C (hg19) ; chrX:g.108696372G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108696372G>C , CM000685.2:g.108696372G>C	GRCh38
NC_000023.10:g.107939602G>C , CM000685.1:g.107939602G>C	GRCh37
NC_000023.9:g.107826258G>C	NCBI36
NG_011977.1:g.261449G>C
NG_011977.2:g.261449G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.5070G>C MANE Select	ENSP00000331902.7:p.Arg1690Ser
ENST00000361603.7:c.5052G>C	ENSP00000354505.2:p.Arg1684Ser
ENST00000510690.2:n.1564G>C
ENST00000644079.1:n.2758G>C
ENST00000328300.10:c.5070G>C	ENSP00000331902.6:p.Arg1690Ser
ENST00000361603.6:c.5052G>C	ENSP00000354505.2:p.Arg1684Ser
ENST00000504541.1:c.295G>C	ENSP00000424845.1:n.295G>C
ENST00000515658.1:c.400G>C
NM_000495.4:c.5052G>C	NP_000486.1:p.Arg1684Ser
NM_033380.2:c.5070G>C	NP_203699.1:p.Arg1690Ser
XM_005262070.2:c.5061G>C	XP_005262127.1:p.Arg1687Ser
XM_006724616.2:c.5070G>C	XP_006724679.1:p.Arg1690Ser
XM_011530849.1:c.4746G>C	XP_011529151.1:p.Arg1582Ser
XM_011530851.1:c.2643G>C	XP_011529153.1:p.Arg881Ser
XM_011530849.2:c.5085G>C	XP_011529151.2:p.Arg1695Ser
XM_017029259.2:c.5076G>C	XP_016884748.1:p.Arg1692Ser
XM_017029260.1:c.5067G>C	XP_016884749.1:p.Arg1689Ser
XM_017029263.2:c.3405G>C	XP_016884752.1:p.Arg1135Ser
NM_000495.5:c.5052G>C	NP_000486.1:p.Arg1684Ser
NM_033380.3:c.5070G>C MANE Select	NP_203699.1:p.Arg1690Ser