Canonical Allele Identifier: CA318806
Gene: SRPX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.100662289C>T , CM000685.2:g.100662289C>T GRCh38
NC_000023.10:g.99917286C>T , CM000685.1:g.99917286C>T GRCh37
NC_000023.9:g.99803942C>T NCBI36
NG_021337.1:g.23124C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373004.5:c.277C>T MANE Select ENSP00000362095.3:p.Arg93Trp
ENST00000638319.1:n.265C>T
ENST00000638458.1:c.301C>T ENSP00000492168.1:p.Arg101Trp
ENST00000638920.1:n.280C>T
ENST00000640020.1:n.582C>T
ENST00000640889.1:c.277C>T ENSP00000492571.1:p.Arg93Trp
ENST00000677630.1:n.211C>T
ENST00000679590.1:n.310C>T
ENST00000373004.3:c.277C>T ENSP00000362095.3:p.Arg93Trp
NM_014467.2:c.277C>T NP_055282.1:p.Arg93Trp
XM_005262121.2:c.277C>T XP_005262178.1:p.Arg93Trp
NM_014467.3:c.277C>T MANE Select NP_055282.1:p.Arg93Trp