Canonical Allele Identifier: CA413851106

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107924121A>T (hg19) ; chrX:g.108680891A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108680891A>T , CM000685.2:g.108680891A>T	GRCh38
NC_000023.10:g.107924121A>T , CM000685.1:g.107924121A>T	GRCh37
NC_000023.9:g.107810777A>T	NCBI36
NG_011977.1:g.245968A>T
NG_011977.2:g.245968A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4022A>T MANE Select	ENSP00000331902.7:p.Lys1341Ile
ENST00000361603.7:c.4004A>T	ENSP00000354505.2:p.Lys1335Ile
ENST00000510690.2:n.516A>T
ENST00000328300.10:c.4022A>T	ENSP00000331902.6:p.Lys1341Ile
ENST00000361603.6:c.4004A>T	ENSP00000354505.2:p.Lys1335Ile
ENST00000489230.1:n.425A>T
NM_000495.4:c.4004A>T	NP_000486.1:p.Lys1335Ile
NM_033380.2:c.4022A>T	NP_203699.1:p.Lys1341Ile
XM_005262070.2:c.4013A>T	XP_005262127.1:p.Lys1338Ile
XM_006724616.2:c.4022A>T	XP_006724679.1:p.Lys1341Ile
XM_011530849.1:c.3698A>T	XP_011529151.1:p.Lys1233Ile
XM_011530851.1:c.1595A>T	XP_011529153.1:p.Lys532Ile
XM_011530849.2:c.4037A>T	XP_011529151.2:p.Lys1346Ile
XM_017029259.2:c.4028A>T	XP_016884748.1:p.Lys1343Ile
XM_017029260.1:c.4019A>T	XP_016884749.1:p.Lys1340Ile
XM_017029263.2:c.2357A>T	XP_016884752.1:p.Lys786Ile
NM_000495.5:c.4004A>T	NP_000486.1:p.Lys1335Ile
NM_033380.3:c.4022A>T MANE Select	NP_203699.1:p.Lys1341Ile