Canonical Allele Identifier: CA6350459

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.125895468C>A , CM000673.2:g.125895468C>A GRCh38
NC_000011.9:g.125765363C>A , CM000673.1:g.125765363C>A GRCh37
NC_000011.8:g.125270573C>A NCBI36
NG_011842.1:g.16855C>A
NG_033067.1:g.12754G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227474.8:c.700G>T (PUS3) MANE Select ENSP00000227474.3:p.Val234Leu
ENST00000425380.7:c.-25-3876C>A (HYLS1) MANE Select ENSP00000414884.2:n.-25-3876C>A
ENST00000227474.7:c.700G>T (PUS3) ENSP00000227474.3:p.Val234Leu
ENST00000356438.7:c.-80-3636C>A (HYLS1) ENSP00000348815.3:n.-80-3636C>A
ENST00000425380.6:c.-25-3876C>A (HYLS1) ENSP00000414884.2:n.-25-3876C>A
ENST00000526028.1:c.-25-3876C>A (HYLS1) ENSP00000436833.1:n.-25-3876C>A
ENST00000530811.5:c.700G>T (PUS3) ENSP00000432386.1:p.Val234Leu
ENST00000613398.4:c.76G>T (PUS3) ENSP00000481536.1:p.Val26Leu
NM_001134793.1:c.-25-3876C>A (HYLS1) NP_001128265.1:n.-25-3876C>A
NM_001271985.1:c.76G>T (PUS3) NP_001258914.1:p.Val26Leu
NM_031307.3:c.700G>T (PUS3) NP_112597.3:p.Val234Leu
NM_145014.2:c.-80-3636C>A (HYLS1) NP_659451.1:n.-80-3636C>A
XM_005271430.2:c.-25-3876C>A (HYLS1) XP_005271487.1:n.-25-3876C>A
XM_005271687.2:c.403G>T (PUS3) XP_005271744.1:p.Val135Leu
XM_005271688.2:c.498+202G>T (PUS3) XP_005271745.1:n.498+202G>T
XM_006718777.2:c.-22-3879C>A (HYLS1) XP_006718840.1:n.-22-3879C>A
XM_006718778.2:c.-22-3879C>A (HYLS1) XP_006718841.1:n.-22-3879C>A
XM_011542657.1:c.-25-3876C>A (HYLS1) XP_011540959.1:n.-25-3876C>A
XM_011542658.1:c.-80-3636C>A (HYLS1) XP_011540960.1:n.-80-3636C>A
XM_011542659.1:c.-25-3876C>A (HYLS1) XP_011540961.1:n.-25-3876C>A
XM_005271688.4:c.498+202G>T (PUS3) XP_005271745.1:n.498+202G>T
XM_006718777.3:c.-22-3879C>A (HYLS1) XP_006718840.1:n.-22-3879C>A
XM_011542659.2:c.-25-3876C>A (HYLS1) XP_011540961.1:n.-25-3876C>A
XM_017017320.1:c.-25-3876C>A (HYLS1) XP_016872809.1:n.-25-3876C>A
XM_017017321.1:c.-22-3879C>A (HYLS1) XP_016872810.1:n.-22-3879C>A
XM_024448706.1:c.403G>T (PUS3) XP_024304474.1:p.Val135Leu
NM_031307.4:c.700G>T (PUS3) MANE Select NP_112597.4:p.Val234Leu
NM_001134793.2:c.-25-3876C>A (HYLS1) MANE Select NP_001128265.1:n.-25-3876C>A
NM_001377269.1:c.-25-3876C>A (HYLS1) NP_001364198.1:n.-25-3876C>A
NM_001377270.1:c.-22-3879C>A (HYLS1) NP_001364199.1:n.-22-3879C>A
NM_001271985.2:c.76G>T (PUS3) NP_001258914.1:p.Val26Leu
NM_145014.3:c.-80-3636C>A (HYLS1) NP_659451.1:n.-80-3636C>A