Canonical Allele Identifier: CA414132709

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938530G>C (hg19) ; chrX:g.108695300G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695300G>C , CM000685.2:g.108695300G>C	GRCh38
NC_000023.10:g.107938530G>C , CM000685.1:g.107938530G>C	GRCh37
NC_000023.9:g.107825186G>C	NCBI36
NG_011977.1:g.260377G>C
NG_011977.2:g.260377G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4855G>C MANE Select	ENSP00000331902.7:p.Ala1619Pro
ENST00000361603.7:c.4837G>C	ENSP00000354505.2:p.Ala1613Pro
ENST00000510690.2:n.1349G>C
ENST00000644079.1:n.1686G>C
ENST00000328300.10:c.4855G>C	ENSP00000331902.6:p.Ala1619Pro
ENST00000361603.6:c.4837G>C	ENSP00000354505.2:p.Ala1613Pro
ENST00000504541.1:c.219+379G>C	ENSP00000424845.1:n.219+379G>C
ENST00000515658.1:c.325-997G>C
NM_000495.4:c.4837G>C	NP_000486.1:p.Ala1613Pro
NM_033380.2:c.4855G>C	NP_203699.1:p.Ala1619Pro
XM_005262070.2:c.4846G>C	XP_005262127.1:p.Ala1616Pro
XM_006724616.2:c.4855G>C	XP_006724679.1:p.Ala1619Pro
XM_011530849.1:c.4531G>C	XP_011529151.1:p.Ala1511Pro
XM_011530851.1:c.2428G>C	XP_011529153.1:p.Ala810Pro
XM_011530849.2:c.4870G>C	XP_011529151.2:p.Ala1624Pro
XM_017029259.2:c.4861G>C	XP_016884748.1:p.Ala1621Pro
XM_017029260.1:c.4852G>C	XP_016884749.1:p.Ala1618Pro
XM_017029263.2:c.3190G>C	XP_016884752.1:p.Ala1064Pro
NM_000495.5:c.4837G>C	NP_000486.1:p.Ala1613Pro
NM_033380.3:c.4855G>C MANE Select	NP_203699.1:p.Ala1619Pro