Canonical Allele Identifier: CA414132587

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938132T>G (hg19) ; chrX:g.108694902T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694902T>G , CM000685.2:g.108694902T>G	GRCh38
NC_000023.10:g.107938132T>G , CM000685.1:g.107938132T>G	GRCh37
NC_000023.9:g.107824788T>G	NCBI36
NG_011977.1:g.259979T>G
NG_011977.2:g.259979T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4802T>G MANE Select	ENSP00000331902.7:p.Ile1601Ser
ENST00000361603.7:c.4784T>G	ENSP00000354505.2:p.Ile1595Ser
ENST00000510690.2:n.1296T>G
ENST00000644079.1:n.1288T>G
ENST00000328300.10:c.4802T>G	ENSP00000331902.6:p.Ile1601Ser
ENST00000361603.6:c.4784T>G	ENSP00000354505.2:p.Ile1595Ser
ENST00000504541.1:c.200T>G	ENSP00000424845.1:p.Ile67Ser
ENST00000515658.1:c.325-1395T>G
NM_000495.4:c.4784T>G	NP_000486.1:p.Ile1595Ser
NM_033380.2:c.4802T>G	NP_203699.1:p.Ile1601Ser
XM_005262070.2:c.4793T>G	XP_005262127.1:p.Ile1598Ser
XM_006724616.2:c.4802T>G	XP_006724679.1:p.Ile1601Ser
XM_011530849.1:c.4478T>G	XP_011529151.1:p.Ile1493Ser
XM_011530851.1:c.2375T>G	XP_011529153.1:p.Ile792Ser
XM_011530849.2:c.4817T>G	XP_011529151.2:p.Ile1606Ser
XM_017029259.2:c.4808T>G	XP_016884748.1:p.Ile1603Ser
XM_017029260.1:c.4799T>G	XP_016884749.1:p.Ile1600Ser
XM_017029263.2:c.3137T>G	XP_016884752.1:p.Ile1046Ser
NM_000495.5:c.4784T>G	NP_000486.1:p.Ile1595Ser
NM_033380.3:c.4802T>G MANE Select	NP_203699.1:p.Ile1601Ser