Canonical Allele Identifier: CA412992591
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 450213
ClinVar RCV Id: RCV000523903
dbSNP Id: rs1555967297

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474546C>T , CM000685.2:g.41474546C>T GRCh38
NC_000023.10:g.41333799C>T , CM000685.1:g.41333799C>T GRCh37
NC_000023.9:g.41218743C>T NCBI36
NG_009112.1:g.32087C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1078C>T ENSP00000340328.3:p.Pro360Ser
ENST00000378220.3:c.1078C>T MANE Select ENSP00000367465.2:p.Pro360Ser
ENST00000378220.2:c.1093C>T ENSP00000367465.1:p.Pro365Ser
ENST00000342595.2:c.1093C>T ENSP00000340328.2:p.Pro365Ser
ENST00000378220.1:c.1093C>T ENSP00000367465.1:p.Pro365Ser
NM_022567.2:c.1093C>T NP_072089.1:p.Pro365Ser
XM_005272632.2:c.1093C>T XP_005272689.1:p.Pro365Ser
XM_017029709.1:c.1093C>T XP_016885198.1:p.Pro365Ser
NM_001378477.3:c.1078C>T MANE Select NP_001365406.2:p.Pro360Ser
NM_022567.3:c.1078C>T NP_072089.2:p.Pro360Ser