Canonical Allele Identifier: CA2693491328

Gene: NYX

Linked Data

• gnomAD v4: X-41474657-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474661del , CM000685.2:g.41474661del	GRCh38
NC_000023.10:g.41333914del , CM000685.1:g.41333914del	GRCh37
NC_000023.9:g.41218858del	NCBI36
NG_009112.1:g.32202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1193del	ENSP00000340328.3:p.Pro398GlnfsTer8
ENST00000378220.3:c.1193del MANE Select	ENSP00000367465.2:p.Pro398GlnfsTer8
ENST00000378220.2:c.1208del	ENSP00000367465.1:p.Pro403GlnfsTer8
ENST00000342595.2:c.1208del	ENSP00000340328.2:p.Pro403GlnfsTer8
ENST00000378220.1:c.1208del	ENSP00000367465.1:p.Pro403GlnfsTer8
NM_022567.2:c.1208del	NP_072089.1:p.Pro403GlnfsTer8
XM_005272632.2:c.1208del	XP_005272689.1:p.Pro403GlnfsTer8
XM_017029709.1:c.1208del	XP_016885198.1:p.Pro403GlnfsTer8
NM_001378477.3:c.1193del MANE Select	NP_001365406.2:p.Pro398GlnfsTer8
NM_022567.3:c.1193del	NP_072089.2:p.Pro398GlnfsTer8