Canonical Allele Identifier: CA414132995

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938661C>G (hg19) ; chrX:g.108695431C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695431C>G , CM000685.2:g.108695431C>G	GRCh38
NC_000023.10:g.107938661C>G , CM000685.1:g.107938661C>G	GRCh37
NC_000023.9:g.107825317C>G	NCBI36
NG_011977.1:g.260508C>G
NG_011977.2:g.260508C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4986C>G MANE Select	ENSP00000331902.7:p.Asp1662Glu
ENST00000361603.7:c.4968C>G	ENSP00000354505.2:p.Asp1656Glu
ENST00000510690.2:n.1480C>G
ENST00000644079.1:n.1817C>G
ENST00000328300.10:c.4986C>G	ENSP00000331902.6:p.Asp1662Glu
ENST00000361603.6:c.4968C>G	ENSP00000354505.2:p.Asp1656Glu
ENST00000504541.1:c.219+510C>G	ENSP00000424845.1:n.219+510C>G
ENST00000515658.1:c.325-866C>G
NM_000495.4:c.4968C>G	NP_000486.1:p.Asp1656Glu
NM_033380.2:c.4986C>G	NP_203699.1:p.Asp1662Glu
XM_005262070.2:c.4977C>G	XP_005262127.1:p.Asp1659Glu
XM_006724616.2:c.4986C>G	XP_006724679.1:p.Asp1662Glu
XM_011530849.1:c.4662C>G	XP_011529151.1:p.Asp1554Glu
XM_011530851.1:c.2559C>G	XP_011529153.1:p.Asp853Glu
XM_011530849.2:c.5001C>G	XP_011529151.2:p.Asp1667Glu
XM_017029259.2:c.4992C>G	XP_016884748.1:p.Asp1664Glu
XM_017029260.1:c.4983C>G	XP_016884749.1:p.Asp1661Glu
XM_017029263.2:c.3321C>G	XP_016884752.1:p.Asp1107Glu
NM_000495.5:c.4968C>G	NP_000486.1:p.Asp1656Glu
NM_033380.3:c.4986C>G MANE Select	NP_203699.1:p.Asp1662Glu