Canonical Allele Identifier: CA517925841

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938109T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694879T>C , CM000685.2:g.108694879T>C	GRCh38
NC_000023.10:g.107938109T>C , CM000685.1:g.107938109T>C	GRCh37
NC_000023.9:g.107824765T>C	NCBI36
NG_011977.1:g.259956T>C
NG_011977.2:g.259956T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4779T>C MANE Select	ENSP00000331902.7:p.Pro1593=
ENST00000361603.7:c.4761T>C	ENSP00000354505.2:p.Pro1587=
ENST00000510690.2:n.1273T>C
ENST00000644079.1:n.1265T>C
ENST00000328300.10:c.4779T>C	ENSP00000331902.6:p.Pro1593=
ENST00000361603.6:c.4761T>C	ENSP00000354505.2:p.Pro1587=
ENST00000504541.1:c.177T>C	ENSP00000424845.1:p.Pro59=
ENST00000515658.1:c.325-1418T>C
NM_000495.4:c.4761T>C	NP_000486.1:p.Pro1587=
NM_033380.2:c.4779T>C	NP_203699.1:p.Pro1593=
XM_005262070.2:c.4770T>C	XP_005262127.1:p.Pro1590=
XM_006724616.2:c.4779T>C	XP_006724679.1:p.Pro1593=
XM_011530849.1:c.4455T>C	XP_011529151.1:p.Pro1485=
XM_011530851.1:c.2352T>C	XP_011529153.1:p.Pro784=
XM_011530849.2:c.4794T>C	XP_011529151.2:p.Pro1598=
XM_017029259.2:c.4785T>C	XP_016884748.1:p.Pro1595=
XM_017029260.1:c.4776T>C	XP_016884749.1:p.Pro1592=
XM_017029263.2:c.3114T>C	XP_016884752.1:p.Pro1038=
NM_000495.5:c.4761T>C	NP_000486.1:p.Pro1587=
NM_033380.3:c.4779T>C MANE Select	NP_203699.1:p.Pro1593=