Canonical Allele Identifier: CA2425928152
Gene: NYX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474637C= , CM000685.2:g.41474637C= GRCh38
NC_000023.10:g.41333890C= , CM000685.1:g.41333890C= GRCh37
NC_000023.9:g.41218834C= NCBI36
NG_009112.1:g.32178C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1169C= ENSP00000340328.3:p.Thr390=
ENST00000378220.3:c.1169C= MANE Select ENSP00000367465.2:p.Thr390=
ENST00000378220.2:c.1184C= ENSP00000367465.1:p.Thr395=
ENST00000342595.2:c.1184C= ENSP00000340328.2:p.Thr395=
ENST00000378220.1:c.1184C= ENSP00000367465.1:p.Thr395=
NM_022567.2:c.1184C= NP_072089.1:p.Thr395=
XM_005272632.2:c.1184C= XP_005272689.1:p.Thr395=
XM_017029709.1:c.1184C= XP_016885198.1:p.Thr395=
NM_001378477.3:c.1169C= MANE Select NP_001365406.2:p.Thr390=
NM_022567.3:c.1169C= NP_072089.2:p.Thr390=