Canonical Allele Identifier: CA414132502

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938094G>T (hg19) ; chrX:g.108694864G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694864G>T , CM000685.2:g.108694864G>T	GRCh38
NC_000023.10:g.107938094G>T , CM000685.1:g.107938094G>T	GRCh37
NC_000023.9:g.107824750G>T	NCBI36
NG_011977.1:g.259941G>T
NG_011977.2:g.259941G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4764G>T MANE Select	ENSP00000331902.7:p.Gln1588His
ENST00000361603.7:c.4746G>T	ENSP00000354505.2:p.Gln1582His
ENST00000510690.2:n.1258G>T
ENST00000644079.1:n.1250G>T
ENST00000328300.10:c.4764G>T	ENSP00000331902.6:p.Gln1588His
ENST00000361603.6:c.4746G>T	ENSP00000354505.2:p.Gln1582His
ENST00000504541.1:c.162G>T	ENSP00000424845.1:p.Gln54His
ENST00000515658.1:c.325-1433G>T
NM_000495.4:c.4746G>T	NP_000486.1:p.Gln1582His
NM_033380.2:c.4764G>T	NP_203699.1:p.Gln1588His
XM_005262070.2:c.4755G>T	XP_005262127.1:p.Gln1585His
XM_006724616.2:c.4764G>T	XP_006724679.1:p.Gln1588His
XM_011530849.1:c.4440G>T	XP_011529151.1:p.Gln1480His
XM_011530851.1:c.2337G>T	XP_011529153.1:p.Gln779His
XM_011530849.2:c.4779G>T	XP_011529151.2:p.Gln1593His
XM_017029259.2:c.4770G>T	XP_016884748.1:p.Gln1590His
XM_017029260.1:c.4761G>T	XP_016884749.1:p.Gln1587His
XM_017029263.2:c.3099G>T	XP_016884752.1:p.Gln1033His
NM_000495.5:c.4746G>T	NP_000486.1:p.Gln1582His
NM_033380.3:c.4764G>T MANE Select	NP_203699.1:p.Gln1588His