Canonical Allele Identifier: CA414132723

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938537C>A (hg19) ; chrX:g.108695307C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695307C>A , CM000685.2:g.108695307C>A	GRCh38
NC_000023.10:g.107938537C>A , CM000685.1:g.107938537C>A	GRCh37
NC_000023.9:g.107825193C>A	NCBI36
NG_011977.1:g.260384C>A
NG_011977.2:g.260384C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4862C>A MANE Select	ENSP00000331902.7:p.Ala1621Asp
ENST00000361603.7:c.4844C>A	ENSP00000354505.2:p.Ala1615Asp
ENST00000510690.2:n.1356C>A
ENST00000644079.1:n.1693C>A
ENST00000328300.10:c.4862C>A	ENSP00000331902.6:p.Ala1621Asp
ENST00000361603.6:c.4844C>A	ENSP00000354505.2:p.Ala1615Asp
ENST00000504541.1:c.219+386C>A	ENSP00000424845.1:n.219+386C>A
ENST00000515658.1:c.325-990C>A
NM_000495.4:c.4844C>A	NP_000486.1:p.Ala1615Asp
NM_033380.2:c.4862C>A	NP_203699.1:p.Ala1621Asp
XM_005262070.2:c.4853C>A	XP_005262127.1:p.Ala1618Asp
XM_006724616.2:c.4862C>A	XP_006724679.1:p.Ala1621Asp
XM_011530849.1:c.4538C>A	XP_011529151.1:p.Ala1513Asp
XM_011530851.1:c.2435C>A	XP_011529153.1:p.Ala812Asp
XM_011530849.2:c.4877C>A	XP_011529151.2:p.Ala1626Asp
XM_017029259.2:c.4868C>A	XP_016884748.1:p.Ala1623Asp
XM_017029260.1:c.4859C>A	XP_016884749.1:p.Ala1620Asp
XM_017029263.2:c.3197C>A	XP_016884752.1:p.Ala1066Asp
NM_000495.5:c.4844C>A	NP_000486.1:p.Ala1615Asp
NM_033380.3:c.4862C>A MANE Select	NP_203699.1:p.Ala1621Asp