Canonical Allele Identifier: CA10469474
Community Standard Title: NM_014467.3(SRPX2):c.356-38G>A
Gene: SRPX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.100664736G>A , CM000685.2:g.100664736G>A GRCh38
NC_000023.10:g.99919733G>A , CM000685.1:g.99919733G>A GRCh37
NC_000023.9:g.99806389G>A NCBI36
NG_021337.1:g.25571G>A

Transcript Alleles

HGVS Amino-acid Change
NM_014467.3:c.356-38G>A MANE Select NP_055282.1:n.356-38G>A
ENST00000373004.5:c.356-38G>A MANE Select ENSP00000362095.3:n.356-38G>A
NM_014467.2:c.356-38G>A NP_055282.1:n.356-38G>A
ENST00000373004.3:c.356-38G>A ENSP00000362095.3:n.356-38G>A
ENST00000638319.1:n.344-38G>A
ENST00000638458.1:c.380-38G>A ENSP00000492168.1:n.380-38G>A
ENST00000638920.1:n.359-38G>A
ENST00000640889.1:c.356-38G>A ENSP00000492571.1:n.356-38G>A
ENST00000677630.1:n.290-38G>A
ENST00000679590.1:n.389-38G>A
XM_005262121.2:c.356-38G>A XP_005262178.1:n.356-38G>A