Canonical Allele Identifier: CA869827290

Gene: COL4A5

Linked Data

• dbSNP Id: rs1384885798
• MyVariant Identifiers: chrX:g.107937894C>T (hg19) ; chrX:g.108694664C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694664C>T , CM000685.2:g.108694664C>T	GRCh38
NC_000023.10:g.107937894C>T , CM000685.1:g.107937894C>T	GRCh37
NC_000023.9:g.107824550C>T	NCBI36
NG_011977.1:g.259741C>T
NG_011977.2:g.259741C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4707-143C>T MANE Select	ENSP00000331902.7:n.4707-143C>T
ENST00000361603.7:c.4689-143C>T	ENSP00000354505.2:n.4689-143C>T
ENST00000510690.2:n.1201-143C>T
ENST00000644079.1:n.1050C>T
ENST00000328300.10:c.4707-143C>T	ENSP00000331902.6:n.4707-143C>T
ENST00000361603.6:c.4689-143C>T	ENSP00000354505.2:n.4689-143C>T
ENST00000504541.1:c.105-143C>T	ENSP00000424845.1:n.105-143C>T
ENST00000515658.1:c.325-1633C>T
NM_000495.4:c.4689-143C>T	NP_000486.1:n.4689-143C>T
NM_033380.2:c.4707-143C>T	NP_203699.1:n.4707-143C>T
XM_005262070.2:c.4698-143C>T	XP_005262127.1:n.4698-143C>T
XM_006724616.2:c.4707-143C>T	XP_006724679.1:n.4707-143C>T
XM_011530849.1:c.4383-143C>T	XP_011529151.1:n.4383-143C>T
XM_011530851.1:c.2280-143C>T	XP_011529153.1:n.2280-143C>T
XM_011530849.2:c.4722-143C>T	XP_011529151.2:n.4722-143C>T
XM_017029259.2:c.4713-143C>T	XP_016884748.1:n.4713-143C>T
XM_017029260.1:c.4704-143C>T	XP_016884749.1:n.4704-143C>T
XM_017029263.2:c.3042-143C>T	XP_016884752.1:n.3042-143C>T
NM_000495.5:c.4689-143C>T	NP_000486.1:n.4689-143C>T
NM_033380.3:c.4707-143C>T MANE Select	NP_203699.1:n.4707-143C>T