Canonical Allele Identifier: CA6350575

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.125896080T>C , CM000673.2:g.125896080T>C GRCh38
NC_000011.9:g.125765975T>C , CM000673.1:g.125765975T>C GRCh37
NC_000011.8:g.125271185T>C NCBI36
NG_011842.1:g.17467T>C
NG_033067.1:g.12142A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227474.8:c.205A>G (PUS3) MANE Select ENSP00000227474.3:p.Ile69Val
ENST00000425380.7:c.-25-3264T>C (HYLS1) MANE Select ENSP00000414884.2:n.-25-3264T>C
ENST00000227474.7:c.205A>G (PUS3) ENSP00000227474.3:p.Ile69Val
ENST00000356438.7:c.-80-3024T>C (HYLS1) ENSP00000348815.3:n.-80-3024T>C
ENST00000425380.6:c.-25-3264T>C (HYLS1) ENSP00000414884.2:n.-25-3264T>C
ENST00000526028.1:c.-25-3264T>C (HYLS1) ENSP00000436833.1:n.-25-3264T>C
ENST00000529801.1:c.205A>G (PUS3) ENSP00000437077.1:p.Ile69Val
ENST00000530811.5:c.205A>G (PUS3) ENSP00000432386.1:p.Ile69Val
ENST00000534158.5:c.205A>G (PUS3) ENSP00000432272.1:p.Ile69Val
ENST00000613398.4:c.-246-291A>G (PUS3) ENSP00000481536.1:n.-246-291A>G
NM_001134793.1:c.-25-3264T>C (HYLS1) NP_001128265.1:n.-25-3264T>C
NM_001271985.1:c.-246-291A>G (PUS3) NP_001258914.1:n.-246-291A>G
NM_031307.3:c.205A>G (PUS3) NP_112597.3:p.Ile69Val
NM_145014.2:c.-80-3024T>C (HYLS1) NP_659451.1:n.-80-3024T>C
XM_005271430.2:c.-25-3264T>C (HYLS1) XP_005271487.1:n.-25-3264T>C
XM_005271687.2:c.82-291A>G (PUS3) XP_005271744.1:n.82-291A>G
XM_005271688.2:c.205A>G (PUS3) XP_005271745.1:p.Ile69Val
XM_006718777.2:c.-22-3267T>C (HYLS1) XP_006718840.1:n.-22-3267T>C
XM_006718778.2:c.-22-3267T>C (HYLS1) XP_006718841.1:n.-22-3267T>C
XM_011542657.1:c.-25-3264T>C (HYLS1) XP_011540959.1:n.-25-3264T>C
XM_011542658.1:c.-80-3024T>C (HYLS1) XP_011540960.1:n.-80-3024T>C
XM_011542659.1:c.-25-3264T>C (HYLS1) XP_011540961.1:n.-25-3264T>C
XM_005271688.4:c.205A>G (PUS3) XP_005271745.1:p.Ile69Val
XM_006718777.3:c.-22-3267T>C (HYLS1) XP_006718840.1:n.-22-3267T>C
XM_011542659.2:c.-25-3264T>C (HYLS1) XP_011540961.1:n.-25-3264T>C
XM_017017320.1:c.-25-3264T>C (HYLS1) XP_016872809.1:n.-25-3264T>C
XM_017017321.1:c.-22-3267T>C (HYLS1) XP_016872810.1:n.-22-3267T>C
XM_024448706.1:c.82-291A>G (PUS3) XP_024304474.1:n.82-291A>G
NM_031307.4:c.205A>G (PUS3) MANE Select NP_112597.4:p.Ile69Val
NM_001134793.2:c.-25-3264T>C (HYLS1) MANE Select NP_001128265.1:n.-25-3264T>C
NM_001377269.1:c.-25-3264T>C (HYLS1) NP_001364198.1:n.-25-3264T>C
NM_001377270.1:c.-22-3267T>C (HYLS1) NP_001364199.1:n.-22-3267T>C
NM_001271985.2:c.-246-291A>G (PUS3) NP_001258914.1:n.-246-291A>G
NM_145014.3:c.-80-3024T>C (HYLS1) NP_659451.1:n.-80-3024T>C