Canonical Allele Identifier: CA413850385

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107920795A>G (hg19) ; chrX:g.108677565A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108677565A>G , CM000685.2:g.108677565A>G	GRCh38
NC_000023.10:g.107920795A>G , CM000685.1:g.107920795A>G	GRCh37
NC_000023.9:g.107807451A>G	NCBI36
NG_011977.1:g.242642A>G
NG_011977.2:g.242642A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.3874A>G MANE Select	ENSP00000331902.7:p.Asn1292Asp
ENST00000361603.7:c.3856A>G	ENSP00000354505.2:p.Asn1286Asp
ENST00000510690.2:n.368A>G
ENST00000328300.10:c.3874A>G	ENSP00000331902.6:p.Asn1292Asp
ENST00000361603.6:c.3856A>G	ENSP00000354505.2:p.Asn1286Asp
ENST00000489230.1:n.277A>G
ENST00000510690.1:n.368A>G
NM_000495.4:c.3856A>G	NP_000486.1:p.Asn1286Asp
NM_033380.2:c.3874A>G	NP_203699.1:p.Asn1292Asp
XM_005262070.2:c.3865A>G	XP_005262127.1:p.Asn1289Asp
XM_006724616.2:c.3874A>G	XP_006724679.1:p.Asn1292Asp
XM_011530849.1:c.3550A>G	XP_011529151.1:p.Asn1184Asp
XM_011530851.1:c.1447A>G	XP_011529153.1:p.Asn483Asp
XM_011530849.2:c.3889A>G	XP_011529151.2:p.Asn1297Asp
XM_017029259.2:c.3880A>G	XP_016884748.1:p.Asn1294Asp
XM_017029260.1:c.3871A>G	XP_016884749.1:p.Asn1291Asp
XM_017029261.1:c.3889A>G	XP_016884750.1:p.Asn1297Asp
XM_017029263.2:c.2209A>G	XP_016884752.1:p.Asn737Asp
NM_000495.5:c.3856A>G	NP_000486.1:p.Asn1286Asp
NM_033380.3:c.3874A>G MANE Select	NP_203699.1:p.Asn1292Asp