Canonical Allele Identifier: CA517923681

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107924179T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108680949T>C , CM000685.2:g.108680949T>C	GRCh38
NC_000023.10:g.107924179T>C , CM000685.1:g.107924179T>C	GRCh37
NC_000023.9:g.107810835T>C	NCBI36
NG_011977.1:g.246026T>C
NG_011977.2:g.246026T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4080T>C MANE Select	ENSP00000331902.7:p.Gly1360=
ENST00000361603.7:c.4062T>C	ENSP00000354505.2:p.Gly1354=
ENST00000510690.2:n.574T>C
ENST00000328300.10:c.4080T>C	ENSP00000331902.6:p.Gly1360=
ENST00000361603.6:c.4062T>C	ENSP00000354505.2:p.Gly1354=
ENST00000489230.1:n.483T>C
NM_000495.4:c.4062T>C	NP_000486.1:p.Gly1354=
NM_033380.2:c.4080T>C	NP_203699.1:p.Gly1360=
XM_005262070.2:c.4071T>C	XP_005262127.1:p.Gly1357=
XM_006724616.2:c.4080T>C	XP_006724679.1:p.Gly1360=
XM_011530849.1:c.3756T>C	XP_011529151.1:p.Gly1252=
XM_011530851.1:c.1653T>C	XP_011529153.1:p.Gly551=
XM_011530849.2:c.4095T>C	XP_011529151.2:p.Gly1365=
XM_017029259.2:c.4086T>C	XP_016884748.1:p.Gly1362=
XM_017029260.1:c.4077T>C	XP_016884749.1:p.Gly1359=
XM_017029263.2:c.2415T>C	XP_016884752.1:p.Gly805=
NM_000495.5:c.4062T>C	NP_000486.1:p.Gly1354=
NM_033380.3:c.4080T>C MANE Select	NP_203699.1:p.Gly1360=