Canonical Allele Identifier: CA412992628
Gene: NYX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474556T>G , CM000685.2:g.41474556T>G GRCh38
NC_000023.10:g.41333809T>G , CM000685.1:g.41333809T>G GRCh37
NC_000023.9:g.41218753T>G NCBI36
NG_009112.1:g.32097T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1088T>G ENSP00000340328.3:p.Val363Gly
ENST00000378220.3:c.1088T>G MANE Select ENSP00000367465.2:p.Val363Gly
ENST00000378220.2:c.1103T>G ENSP00000367465.1:p.Val368Gly
ENST00000342595.2:c.1103T>G ENSP00000340328.2:p.Val368Gly
ENST00000378220.1:c.1103T>G ENSP00000367465.1:p.Val368Gly
NM_022567.2:c.1103T>G NP_072089.1:p.Val368Gly
XM_005272632.2:c.1103T>G XP_005272689.1:p.Val368Gly
XM_017029709.1:c.1103T>G XP_016885198.1:p.Val368Gly
NM_001378477.3:c.1088T>G MANE Select NP_001365406.2:p.Val363Gly
NM_022567.3:c.1088T>G NP_072089.2:p.Val363Gly