Canonical Allele Identifier: CA2545649389

Gene: NYX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474525_41474526insG , CM000685.2:g.41474525_41474526insG	GRCh38
NC_000023.10:g.41333778_41333779insG , CM000685.1:g.41333778_41333779insG	GRCh37
NC_000023.9:g.41218722_41218723insG	NCBI36
NG_009112.1:g.32066_32067insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1057_1058insG	ENSP00000340328.3:p.Thr353SerfsTer?
ENST00000378220.3:c.1057_1058insG MANE Select	ENSP00000367465.2:p.Thr353SerfsTer?
ENST00000378220.2:c.1072_1073insG	ENSP00000367465.1:p.Thr358SerfsTer?
ENST00000342595.2:c.1072_1073insG	ENSP00000340328.2:p.Thr358SerfsTer?
ENST00000378220.1:c.1072_1073insG	ENSP00000367465.1:p.Thr358SerfsTer?
NM_022567.2:c.1072_1073insG	NP_072089.1:p.Thr358SerfsTer?
XM_005272632.2:c.1072_1073insG	XP_005272689.1:p.Thr358SerfsTer?
XM_017029709.1:c.1072_1073insG	XP_016885198.1:p.Thr358SerfsTer?
NM_001378477.3:c.1057_1058insG MANE Select	NP_001365406.2:p.Thr353SerfsTer?
NM_022567.3:c.1057_1058insG	NP_072089.2:p.Thr353SerfsTer?