Canonical Allele Identifier: CA413846903

Gene: COL4A5

Linked Data

• gnomAD v4: X-108601890-C-T
• MyVariant Identifiers: chrX:g.107845120C>T (hg19) ; chrX:g.108601890C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108601890C>T , CM000685.2:g.108601890C>T	GRCh38
NC_000023.10:g.107845120C>T , CM000685.1:g.107845120C>T	GRCh37
NC_000023.9:g.107731776C>T	NCBI36
NG_011977.1:g.166967C>T
NG_011977.2:g.166967C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.2047C>T MANE Select	ENSP00000331902.7:p.Pro683Ser
ENST00000361603.7:c.2047C>T	ENSP00000354505.2:p.Pro683Ser
ENST00000328300.10:c.2047C>T	ENSP00000331902.6:p.Pro683Ser
ENST00000361603.6:c.2047C>T	ENSP00000354505.2:p.Pro683Ser
ENST00000483338.1:n.1503C>T
NM_000495.4:c.2047C>T	NP_000486.1:p.Pro683Ser
NM_033380.2:c.2047C>T	NP_203699.1:p.Pro683Ser
XM_005262070.2:c.2047C>T	XP_005262127.1:p.Pro683Ser
XM_005262072.3:c.2047C>T	XP_005262129.1:p.Pro683Ser
XM_006724616.2:c.2047C>T	XP_006724679.1:p.Pro683Ser
XM_011530849.1:c.1723C>T	XP_011529151.1:p.Pro575Ser
XM_011530850.1:c.2047C>T	XP_011529152.1:p.Pro683Ser
XM_011530849.2:c.2062C>T	XP_011529151.2:p.Pro688Ser
XM_017029259.2:c.2062C>T	XP_016884748.1:p.Pro688Ser
XM_017029260.1:c.2062C>T	XP_016884749.1:p.Pro688Ser
XM_017029261.1:c.2062C>T	XP_016884750.1:p.Pro688Ser
XM_017029262.2:c.2062C>T	XP_016884751.1:p.Pro688Ser
XM_017029263.2:c.382C>T	XP_016884752.1:p.Pro128Ser
NM_000495.5:c.2047C>T	NP_000486.1:p.Pro683Ser
NM_033380.3:c.2047C>T MANE Select	NP_203699.1:p.Pro683Ser