Canonical Allele Identifier: CA517925559

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938046A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694816A>T , CM000685.2:g.108694816A>T	GRCh38
NC_000023.10:g.107938046A>T , CM000685.1:g.107938046A>T	GRCh37
NC_000023.9:g.107824702A>T	NCBI36
NG_011977.1:g.259893A>T
NG_011977.2:g.259893A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4716A>T MANE Select	ENSP00000331902.7:p.Val1572=
ENST00000361603.7:c.4698A>T	ENSP00000354505.2:p.Val1566=
ENST00000510690.2:n.1210A>T
ENST00000644079.1:n.1202A>T
ENST00000328300.10:c.4716A>T	ENSP00000331902.6:p.Val1572=
ENST00000361603.6:c.4698A>T	ENSP00000354505.2:p.Val1566=
ENST00000504541.1:c.114A>T	ENSP00000424845.1:p.Val38=
ENST00000515658.1:c.325-1481A>T
NM_000495.4:c.4698A>T	NP_000486.1:p.Val1566=
NM_033380.2:c.4716A>T	NP_203699.1:p.Val1572=
XM_005262070.2:c.4707A>T	XP_005262127.1:p.Val1569=
XM_006724616.2:c.4716A>T	XP_006724679.1:p.Val1572=
XM_011530849.1:c.4392A>T	XP_011529151.1:p.Val1464=
XM_011530851.1:c.2289A>T	XP_011529153.1:p.Val763=
XM_011530849.2:c.4731A>T	XP_011529151.2:p.Val1577=
XM_017029259.2:c.4722A>T	XP_016884748.1:p.Val1574=
XM_017029260.1:c.4713A>T	XP_016884749.1:p.Val1571=
XM_017029263.2:c.3051A>T	XP_016884752.1:p.Val1017=
NM_000495.5:c.4698A>T	NP_000486.1:p.Val1566=
NM_033380.3:c.4716A>T MANE Select	NP_203699.1:p.Val1572=