Canonical Allele Identifier: CA413852055

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107925033T>G (hg19) ; chrX:g.108681803T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108681803T>G , CM000685.2:g.108681803T>G	GRCh38
NC_000023.10:g.107925033T>G , CM000685.1:g.107925033T>G	GRCh37
NC_000023.9:g.107811689T>G	NCBI36
NG_011977.1:g.246880T>G
NG_011977.2:g.246880T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4131T>G MANE Select	ENSP00000331902.7:p.Ile1377Met
ENST00000361603.7:c.4113T>G	ENSP00000354505.2:p.Ile1371Met
ENST00000510690.2:n.625T>G
ENST00000328300.10:c.4131T>G	ENSP00000331902.6:p.Ile1377Met
ENST00000361603.6:c.4113T>G	ENSP00000354505.2:p.Ile1371Met
ENST00000489230.1:n.534T>G
NM_000495.4:c.4113T>G	NP_000486.1:p.Ile1371Met
NM_033380.2:c.4131T>G	NP_203699.1:p.Ile1377Met
XM_005262070.2:c.4122T>G	XP_005262127.1:p.Ile1374Met
XM_006724616.2:c.4131T>G	XP_006724679.1:p.Ile1377Met
XM_011530849.1:c.3807T>G	XP_011529151.1:p.Ile1269Met
XM_011530851.1:c.1704T>G	XP_011529153.1:p.Ile568Met
XM_011530849.2:c.4146T>G	XP_011529151.2:p.Ile1382Met
XM_017029259.2:c.4137T>G	XP_016884748.1:p.Ile1379Met
XM_017029260.1:c.4128T>G	XP_016884749.1:p.Ile1376Met
XM_017029263.2:c.2466T>G	XP_016884752.1:p.Ile822Met
NM_000495.5:c.4113T>G	NP_000486.1:p.Ile1371Met
NM_033380.3:c.4131T>G MANE Select	NP_203699.1:p.Ile1377Met