Canonical Allele Identifier: CA414132595

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938138A>C (hg19) ; chrX:g.108694908A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694908A>C , CM000685.2:g.108694908A>C	GRCh38
NC_000023.10:g.107938138A>C , CM000685.1:g.107938138A>C	GRCh37
NC_000023.9:g.107824794A>C	NCBI36
NG_011977.1:g.259985A>C
NG_011977.2:g.259985A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4808A>C MANE Select	ENSP00000331902.7:p.Tyr1603Ser
ENST00000361603.7:c.4790A>C	ENSP00000354505.2:p.Tyr1597Ser
ENST00000510690.2:n.1302A>C
ENST00000644079.1:n.1294A>C
ENST00000328300.10:c.4808A>C	ENSP00000331902.6:p.Tyr1603Ser
ENST00000361603.6:c.4790A>C	ENSP00000354505.2:p.Tyr1597Ser
ENST00000504541.1:c.206A>C	ENSP00000424845.1:p.Tyr69Ser
ENST00000515658.1:c.325-1389A>C
NM_000495.4:c.4790A>C	NP_000486.1:p.Tyr1597Ser
NM_033380.2:c.4808A>C	NP_203699.1:p.Tyr1603Ser
XM_005262070.2:c.4799A>C	XP_005262127.1:p.Tyr1600Ser
XM_006724616.2:c.4808A>C	XP_006724679.1:p.Tyr1603Ser
XM_011530849.1:c.4484A>C	XP_011529151.1:p.Tyr1495Ser
XM_011530851.1:c.2381A>C	XP_011529153.1:p.Tyr794Ser
XM_011530849.2:c.4823A>C	XP_011529151.2:p.Tyr1608Ser
XM_017029259.2:c.4814A>C	XP_016884748.1:p.Tyr1605Ser
XM_017029260.1:c.4805A>C	XP_016884749.1:p.Tyr1602Ser
XM_017029263.2:c.3143A>C	XP_016884752.1:p.Tyr1048Ser
NM_000495.5:c.4790A>C	NP_000486.1:p.Tyr1597Ser
NM_033380.3:c.4808A>C MANE Select	NP_203699.1:p.Tyr1603Ser