Canonical Allele Identifier: CA413931354
Community Standard Title: NM_014467.3(SRPX2):c.329G>A (p.Arg110His)
Gene: SRPX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.100662341G>A , CM000685.2:g.100662341G>A GRCh38
NC_000023.10:g.99917338G>A , CM000685.1:g.99917338G>A GRCh37
NC_000023.9:g.99803994G>A NCBI36
NG_021337.1:g.23176G>A

Transcript Alleles

HGVS Amino-acid Change
NM_014467.3:c.329G>A MANE Select NP_055282.1:p.Arg110His
ENST00000373004.5:c.329G>A MANE Select ENSP00000362095.3:p.Arg110His
NM_014467.2:c.329G>A NP_055282.1:p.Arg110His
ENST00000373004.3:c.329G>A ENSP00000362095.3:p.Arg110His
ENST00000638319.1:n.317G>A
ENST00000638458.1:c.353G>A ENSP00000492168.1:p.Arg118His
ENST00000638920.1:n.332G>A
ENST00000640889.1:c.329G>A ENSP00000492571.1:p.Arg110His
ENST00000677630.1:n.263G>A
ENST00000679590.1:n.362G>A
XM_005262121.2:c.329G>A XP_005262178.1:p.Arg110His