Canonical Allele Identifier: CA412992865
Gene: NYX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.41333865G>C (hg19) chrX:g.41474612G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474612G>C , CM000685.2:g.41474612G>C GRCh38
NC_000023.10:g.41333865G>C , CM000685.1:g.41333865G>C GRCh37
NC_000023.9:g.41218809G>C NCBI36
NG_009112.1:g.32153G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1144G>C ENSP00000340328.3:p.Val382Leu
ENST00000378220.3:c.1144G>C MANE Select ENSP00000367465.2:p.Val382Leu
ENST00000378220.2:c.1159G>C ENSP00000367465.1:p.Val387Leu
ENST00000342595.2:c.1159G>C ENSP00000340328.2:p.Val387Leu
ENST00000378220.1:c.1159G>C ENSP00000367465.1:p.Val387Leu
NM_022567.2:c.1159G>C NP_072089.1:p.Val387Leu
XM_005272632.2:c.1159G>C XP_005272689.1:p.Val387Leu
XM_017029709.1:c.1159G>C XP_016885198.1:p.Val387Leu
NM_001378477.3:c.1144G>C MANE Select NP_001365406.2:p.Val382Leu
NM_022567.3:c.1144G>C NP_072089.2:p.Val382Leu
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