Canonical Allele Identifier: CA414132907

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938621A>T (hg19) ; chrX:g.108695391A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695391A>T , CM000685.2:g.108695391A>T	GRCh38
NC_000023.10:g.107938621A>T , CM000685.1:g.107938621A>T	GRCh37
NC_000023.9:g.107825277A>T	NCBI36
NG_011977.1:g.260468A>T
NG_011977.2:g.260468A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4946A>T MANE Select	ENSP00000331902.7:p.Asn1649Ile
ENST00000361603.7:c.4928A>T	ENSP00000354505.2:p.Asn1643Ile
ENST00000510690.2:n.1440A>T
ENST00000644079.1:n.1777A>T
ENST00000328300.10:c.4946A>T	ENSP00000331902.6:p.Asn1649Ile
ENST00000361603.6:c.4928A>T	ENSP00000354505.2:p.Asn1643Ile
ENST00000504541.1:c.219+470A>T	ENSP00000424845.1:n.219+470A>T
ENST00000515658.1:c.325-906A>T
NM_000495.4:c.4928A>T	NP_000486.1:p.Asn1643Ile
NM_033380.2:c.4946A>T	NP_203699.1:p.Asn1649Ile
XM_005262070.2:c.4937A>T	XP_005262127.1:p.Asn1646Ile
XM_006724616.2:c.4946A>T	XP_006724679.1:p.Asn1649Ile
XM_011530849.1:c.4622A>T	XP_011529151.1:p.Asn1541Ile
XM_011530851.1:c.2519A>T	XP_011529153.1:p.Asn840Ile
XM_011530849.2:c.4961A>T	XP_011529151.2:p.Asn1654Ile
XM_017029259.2:c.4952A>T	XP_016884748.1:p.Asn1651Ile
XM_017029260.1:c.4943A>T	XP_016884749.1:p.Asn1648Ile
XM_017029263.2:c.3281A>T	XP_016884752.1:p.Asn1094Ile
NM_000495.5:c.4928A>T	NP_000486.1:p.Asn1643Ile
NM_033380.3:c.4946A>T MANE Select	NP_203699.1:p.Asn1649Ile