Canonical Allele Identifier: CA413852052

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107925032T>C (hg19) ; chrX:g.108681802T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108681802T>C , CM000685.2:g.108681802T>C	GRCh38
NC_000023.10:g.107925032T>C , CM000685.1:g.107925032T>C	GRCh37
NC_000023.9:g.107811688T>C	NCBI36
NG_011977.1:g.246879T>C
NG_011977.2:g.246879T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4130T>C MANE Select	ENSP00000331902.7:p.Ile1377Thr
ENST00000361603.7:c.4112T>C	ENSP00000354505.2:p.Ile1371Thr
ENST00000510690.2:n.624T>C
ENST00000328300.10:c.4130T>C	ENSP00000331902.6:p.Ile1377Thr
ENST00000361603.6:c.4112T>C	ENSP00000354505.2:p.Ile1371Thr
ENST00000489230.1:n.533T>C
NM_000495.4:c.4112T>C	NP_000486.1:p.Ile1371Thr
NM_033380.2:c.4130T>C	NP_203699.1:p.Ile1377Thr
XM_005262070.2:c.4121T>C	XP_005262127.1:p.Ile1374Thr
XM_006724616.2:c.4130T>C	XP_006724679.1:p.Ile1377Thr
XM_011530849.1:c.3806T>C	XP_011529151.1:p.Ile1269Thr
XM_011530851.1:c.1703T>C	XP_011529153.1:p.Ile568Thr
XM_011530849.2:c.4145T>C	XP_011529151.2:p.Ile1382Thr
XM_017029259.2:c.4136T>C	XP_016884748.1:p.Ile1379Thr
XM_017029260.1:c.4127T>C	XP_016884749.1:p.Ile1376Thr
XM_017029263.2:c.2465T>C	XP_016884752.1:p.Ile822Thr
NM_000495.5:c.4112T>C	NP_000486.1:p.Ile1371Thr
NM_033380.3:c.4130T>C MANE Select	NP_203699.1:p.Ile1377Thr