Canonical Allele Identifier: CA10389900
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 2059548
ClinVar RCV Id: RCV002952858
dbSNP Id: rs745741032
gnomAD v2: X-41333757-A-C
gnomAD v3: X-41474504-A-C
gnomAD v4: X-41474504-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474504A>C , CM000685.2:g.41474504A>C GRCh38
NC_000023.10:g.41333757A>C , CM000685.1:g.41333757A>C GRCh37
NC_000023.9:g.41218701A>C NCBI36
NG_009112.1:g.32045A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1036A>C ENSP00000340328.3:p.Met346Leu
ENST00000378220.3:c.1036A>C MANE Select ENSP00000367465.2:p.Met346Leu
ENST00000378220.2:c.1051A>C ENSP00000367465.1:p.Met351Leu
ENST00000342595.2:c.1051A>C ENSP00000340328.2:p.Met351Leu
ENST00000378220.1:c.1051A>C ENSP00000367465.1:p.Met351Leu
NM_022567.2:c.1051A>C NP_072089.1:p.Met351Leu
XM_005272632.2:c.1051A>C XP_005272689.1:p.Met351Leu
XM_017029709.1:c.1051A>C XP_016885198.1:p.Met351Leu
NM_001378477.3:c.1036A>C MANE Select NP_001365406.2:p.Met346Leu
NM_022567.3:c.1036A>C NP_072089.2:p.Met346Leu