Canonical Allele Identifier: CA337491771
Gene: EIF1AY HGNC NCBI

Linked Data

dbSNP Id: rs11422516
gnomAD v3: Y-20583296-G-GC
gnomAD v4: Y-20583296-G-GC
MyVariant Identifiers: chrY:g.22745182_22745183insC (hg19) chrY:g.20583296_20583297insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20583298dup , CM000686.2:g.20583298dup GRCh38
NC_000024.9:g.22745184dup , CM000686.1:g.22745184dup GRCh37
NC_000024.8:g.21154572dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361365.7:c.204+605dup MANE Select ENSP00000354722.2:n.204+605dup
ENST00000361365.6:c.204+605dup ENSP00000354722.2:n.204+605dup
ENST00000382772.3:c.204+605dup ENSP00000372222.3:n.204+605dup
ENST00000465253.1:n.298+605dup
NM_001278612.1:c.204+605dup NP_001265541.1:n.204+605dup
NM_004681.3:c.204+605dup NP_004672.2:n.204+605dup
NM_004681.4:c.204+605dup MANE Select NP_004672.2:n.204+605dup
NM_001278612.2:c.204+605dup NP_001265541.1:n.204+605dup
Search 100 bp 5'
Search 100 bp 3'