Canonical Allele Identifier: CA412992676
Gene: NYX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474570C>G , CM000685.2:g.41474570C>G GRCh38
NC_000023.10:g.41333823C>G , CM000685.1:g.41333823C>G GRCh37
NC_000023.9:g.41218767C>G NCBI36
NG_009112.1:g.32111C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1102C>G ENSP00000340328.3:p.Leu368Val
ENST00000378220.3:c.1102C>G MANE Select ENSP00000367465.2:p.Leu368Val
ENST00000378220.2:c.1117C>G ENSP00000367465.1:p.Leu373Val
ENST00000342595.2:c.1117C>G ENSP00000340328.2:p.Leu373Val
ENST00000378220.1:c.1117C>G ENSP00000367465.1:p.Leu373Val
NM_022567.2:c.1117C>G NP_072089.1:p.Leu373Val
XM_005272632.2:c.1117C>G XP_005272689.1:p.Leu373Val
XM_017029709.1:c.1117C>G XP_016885198.1:p.Leu373Val
NM_001378477.3:c.1102C>G MANE Select NP_001365406.2:p.Leu368Val
NM_022567.3:c.1102C>G NP_072089.2:p.Leu368Val