Canonical Allele Identifier: CA412993382

Gene: NYX

Linked Data

• dbSNP Id: rs1487079098
• gnomAD v2: X-41333980-T-C
• gnomAD v3: X-41474727-T-C
• gnomAD v4: X-41474727-T-C
• MyVariant Identifiers: chrX:g.41333980T>C (hg19) ; chrX:g.41474727T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474727T>C , CM000685.2:g.41474727T>C	GRCh38
NC_000023.10:g.41333980T>C , CM000685.1:g.41333980T>C	GRCh37
NC_000023.9:g.41218924T>C	NCBI36
NG_009112.1:g.32268T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1259T>C	ENSP00000340328.3:p.Val420Ala
ENST00000378220.3:c.1259T>C MANE Select	ENSP00000367465.2:p.Val420Ala
ENST00000378220.2:c.1274T>C	ENSP00000367465.1:p.Val425Ala
ENST00000342595.2:c.1274T>C	ENSP00000340328.2:p.Val425Ala
ENST00000378220.1:c.1274T>C	ENSP00000367465.1:p.Val425Ala
NM_022567.2:c.1274T>C	NP_072089.1:p.Val425Ala
XM_005272632.2:c.1274T>C	XP_005272689.1:p.Val425Ala
XM_017029709.1:c.1274T>C	XP_016885198.1:p.Val425Ala
NM_001378477.3:c.1259T>C MANE Select	NP_001365406.2:p.Val420Ala
NM_022567.3:c.1259T>C	NP_072089.2:p.Val420Ala