Canonical Allele Identifier: CA412992492
Gene: NYX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474516G>C , CM000685.2:g.41474516G>C GRCh38
NC_000023.10:g.41333769G>C , CM000685.1:g.41333769G>C GRCh37
NC_000023.9:g.41218713G>C NCBI36
NG_009112.1:g.32057G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1048G>C ENSP00000340328.3:p.Gly350Arg
ENST00000378220.3:c.1048G>C MANE Select ENSP00000367465.2:p.Gly350Arg
ENST00000378220.2:c.1063G>C ENSP00000367465.1:p.Gly355Arg
ENST00000342595.2:c.1063G>C ENSP00000340328.2:p.Gly355Arg
ENST00000378220.1:c.1063G>C ENSP00000367465.1:p.Gly355Arg
NM_022567.2:c.1063G>C NP_072089.1:p.Gly355Arg
XM_005272632.2:c.1063G>C XP_005272689.1:p.Gly355Arg
XM_017029709.1:c.1063G>C XP_016885198.1:p.Gly355Arg
NM_001378477.3:c.1048G>C MANE Select NP_001365406.2:p.Gly350Arg
NM_022567.3:c.1048G>C NP_072089.2:p.Gly350Arg