Canonical Allele Identifier: CA413854172

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107930789G>C (hg19) ; chrX:g.108687559G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687559G>C , CM000685.2:g.108687559G>C	GRCh38
NC_000023.10:g.107930789G>C , CM000685.1:g.107930789G>C	GRCh37
NC_000023.9:g.107817445G>C	NCBI36
NG_011977.1:g.252636G>C
NG_011977.2:g.252636G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4393G>C MANE Select	ENSP00000331902.7:p.Ala1465Pro
ENST00000361603.7:c.4375G>C	ENSP00000354505.2:p.Ala1459Pro
ENST00000510690.2:n.887G>C
ENST00000328300.10:c.4393G>C	ENSP00000331902.6:p.Ala1465Pro
ENST00000361603.6:c.4375G>C	ENSP00000354505.2:p.Ala1459Pro
ENST00000515658.1:c.189G>C
NM_000495.4:c.4375G>C	NP_000486.1:p.Ala1459Pro
NM_033380.2:c.4393G>C	NP_203699.1:p.Ala1465Pro
XM_005262070.2:c.4384G>C	XP_005262127.1:p.Ala1462Pro
XM_006724616.2:c.4393G>C	XP_006724679.1:p.Ala1465Pro
XM_011530849.1:c.4069G>C	XP_011529151.1:p.Ala1357Pro
XM_011530851.1:c.1966G>C	XP_011529153.1:p.Ala656Pro
XM_011530849.2:c.4408G>C	XP_011529151.2:p.Ala1470Pro
XM_017029259.2:c.4399G>C	XP_016884748.1:p.Ala1467Pro
XM_017029260.1:c.4390G>C	XP_016884749.1:p.Ala1464Pro
XM_017029263.2:c.2728G>C	XP_016884752.1:p.Ala910Pro
NM_000495.5:c.4375G>C	NP_000486.1:p.Ala1459Pro
NM_033380.3:c.4393G>C MANE Select	NP_203699.1:p.Ala1465Pro