Canonical Allele Identifier: CA413849058

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107911701A>G (hg19) ; chrX:g.108668471A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108668471A>G , CM000685.2:g.108668471A>G	GRCh38
NC_000023.10:g.107911701A>G , CM000685.1:g.107911701A>G	GRCh37
NC_000023.9:g.107798357A>G	NCBI36
NG_011977.1:g.233548A>G
NG_011977.2:g.233548A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.3757A>G MANE Select	ENSP00000331902.7:p.Asn1253Asp
ENST00000361603.7:c.3757A>G	ENSP00000354505.2:p.Asn1253Asp
ENST00000328300.10:c.3757A>G	ENSP00000331902.6:p.Asn1253Asp
ENST00000361603.6:c.3757A>G	ENSP00000354505.2:p.Asn1253Asp
NM_000495.4:c.3757A>G	NP_000486.1:p.Asn1253Asp
NM_033380.2:c.3757A>G	NP_203699.1:p.Asn1253Asp
XM_005262070.2:c.3757A>G	XP_005262127.1:p.Asn1253Asp
XM_006724616.2:c.3757A>G	XP_006724679.1:p.Asn1253Asp
XM_011530849.1:c.3433A>G	XP_011529151.1:p.Asn1145Asp
XM_011530850.1:c.3757A>G	XP_011529152.1:p.Asn1253Asp
XM_011530851.1:c.1330A>G	XP_011529153.1:p.Asn444Asp
XM_011530849.2:c.3772A>G	XP_011529151.2:p.Asn1258Asp
XM_017029259.2:c.3772A>G	XP_016884748.1:p.Asn1258Asp
XM_017029260.1:c.3772A>G	XP_016884749.1:p.Asn1258Asp
XM_017029261.1:c.3772A>G	XP_016884750.1:p.Asn1258Asp
XM_017029262.2:c.3772A>G	XP_016884751.1:p.Asn1258Asp
XM_017029263.2:c.2092A>G	XP_016884752.1:p.Asn698Asp
NM_000495.5:c.3757A>G	NP_000486.1:p.Asn1253Asp
NM_033380.3:c.3757A>G MANE Select	NP_203699.1:p.Asn1253Asp