Canonical Allele Identifier: CA333079342
Gene: SRPX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.100662018T>G , CM000685.2:g.100662018T>G GRCh38
NC_000023.10:g.99917015T>G , CM000685.1:g.99917015T>G GRCh37
NC_000023.9:g.99803671T>G NCBI36
NG_021337.1:g.22853T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373004.5:c.164-158T>G MANE Select ENSP00000362095.3:n.164-158T>G
ENST00000638319.1:n.152-158T>G
ENST00000638458.1:c.164-134T>G ENSP00000492168.1:n.164-134T>G
ENST00000638920.1:n.167-158T>G
ENST00000640020.1:n.469-158T>G
ENST00000640889.1:c.164-158T>G ENSP00000492571.1:n.164-158T>G
ENST00000677630.1:n.98-158T>G
ENST00000679590.1:n.39T>G
ENST00000373004.3:c.164-158T>G ENSP00000362095.3:n.164-158T>G
NM_014467.2:c.164-158T>G NP_055282.1:n.164-158T>G
XM_005262121.2:c.164-158T>G XP_005262178.1:n.164-158T>G
NM_014467.3:c.164-158T>G MANE Select NP_055282.1:n.164-158T>G