Canonical Allele Identifier: CA293770
Community Standard Title: NM_014467.3(SRPX2):c.163+12T>C
Gene: SRPX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.100650877T>C , CM000685.2:g.100650877T>C GRCh38
NC_000023.10:g.99905874T>C , CM000685.1:g.99905874T>C GRCh37
NC_000023.9:g.99792530T>C NCBI36
NG_021337.1:g.11712T>C

Transcript Alleles

HGVS Amino-acid Change
NM_014467.3:c.163+12T>C MANE Select NP_055282.1:n.163+12T>C
ENST00000373004.5:c.163+12T>C MANE Select ENSP00000362095.3:n.163+12T>C
NM_014467.2:c.163+12T>C NP_055282.1:n.163+12T>C
ENST00000373004.3:c.163+12T>C ENSP00000362095.3:n.163+12T>C
ENST00000481988.1:n.471T>C
ENST00000638319.1:n.151+12T>C
ENST00000638458.1:c.163+12T>C ENSP00000492168.1:n.163+12T>C
ENST00000638920.1:n.166+12T>C
ENST00000640020.1:n.398+12T>C
ENST00000640889.1:c.163+12T>C ENSP00000492571.1:n.163+12T>C
ENST00000677630.1:n.97+12T>C
XM_005262121.2:c.163+12T>C XP_005262178.1:n.163+12T>C