Canonical Allele Identifier: CA414987771
Gene: DDX3Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12915757T>C , CM000686.2:g.12915757T>C GRCh38
NC_000024.9:g.15027669T>C , CM000686.1:g.15027669T>C GRCh37
NC_000024.8:g.13537063T>C NCBI36
NG_012831.1:g.16651T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.1147T>C MANE Select ENSP00000336725.3:p.Phe383Leu
ENST00000336079.7:c.1147T>C ENSP00000336725.3:p.Phe383Leu
ENST00000360160.8:c.1147T>C ENSP00000353284.4:p.Phe383Leu
ENST00000495478.1:n.262T>C
NM_001122665.2:c.1147T>C NP_001116137.1:p.Phe383Leu
NM_001302552.1:c.1138T>C NP_001289481.1:p.Phe380Leu
NM_004660.4:c.1147T>C NP_004651.2:p.Phe383Leu
XM_006724878.1:c.1147T>C XP_006724941.1:p.Phe383Leu
XM_011531471.1:c.1147T>C XP_011529773.1:p.Phe383Leu
NM_001122665.3:c.1147T>C NP_001116137.1:p.Phe383Leu
NM_001302552.2:c.1138T>C NP_001289481.1:p.Phe380Leu
NM_001324195.1:c.1147T>C NP_001311124.1:p.Phe383Leu
NR_136716.1:n.1616T>C
NR_136717.1:n.1378T>C
NR_136718.1:n.1696T>C
NR_136719.1:n.1486T>C
NR_136720.1:n.1616T>C
NR_136721.1:n.1209T>C
NR_136722.1:n.1293T>C
NR_136723.1:n.1611T>C
NR_136724.1:n.1531T>C
XR_001756014.2:n.1251T>C
NM_004660.5:c.1147T>C MANE Select NP_004651.2:p.Phe383Leu
NM_001302552.3:c.1138T>C NP_001289481.1:p.Phe380Leu
NM_001324195.2:c.1147T>C NP_001311124.1:p.Phe383Leu
NR_136716.2:n.1534T>C
NR_136717.2:n.1296T>C
NR_136718.2:n.1614T>C
NR_136719.2:n.1404T>C
NR_136720.2:n.1534T>C
NR_136721.2:n.1199T>C