Canonical Allele Identifier: CA224287090
Gene: NADSYN1 HGNC NCBI

Linked Data

dbSNP Id: rs1006700472
gnomAD v2: 11-71167472-G-A
gnomAD v3: 11-71456426-G-A
gnomAD v4: 11-71456426-G-A
MyVariant Identifiers: chr11:g.71167472G>A (hg19) chr11:g.71456426G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71456426G>A , CM000673.2:g.71456426G>A GRCh38
NC_000011.9:g.71167472G>A , CM000673.1:g.71167472G>A GRCh37
NC_000011.8:g.70845120G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000319023.7:c.146+1256G>A MANE Select ENSP00000326424.2:n.146+1256G>A
ENST00000319023.6:c.146+1256G>A ENSP00000326424.2:n.146+1256G>A
ENST00000524949.5:n.212+1256G>A
ENST00000525200.5:c.46+1256G>A
ENST00000525245.1:n.87+1256G>A
ENST00000527538.5:n.202+1256G>A
ENST00000528509.5:c.146+1256G>A ENSP00000433472.1:n.146+1256G>A
ENST00000529120.5:c.146+1256G>A ENSP00000437220.1:n.146+1256G>A
ENST00000533769.5:n.212+1256G>A
ENST00000534634.5:n.334+1256G>A
NM_018161.4:c.146+1256G>A NP_060631.2:n.146+1256G>A
NM_018161.5:c.146+1256G>A MANE Select NP_060631.2:n.146+1256G>A
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