Canonical Allele Identifier: CA414854813
Gene: EIF1AY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22741548G>T (hg19) chrY:g.20579662G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20579662G>T , CM000686.2:g.20579662G>T GRCh38
NC_000024.9:g.22741548G>T , CM000686.1:g.22741548G>T GRCh37
NC_000024.8:g.21150936G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361365.7:c.71G>T MANE Select ENSP00000354722.2:p.Arg24Ile
ENST00000361365.6:c.71G>T ENSP00000354722.2:p.Arg24Ile
ENST00000382772.3:c.71G>T ENSP00000372222.3:p.Arg24Ile
ENST00000465253.1:n.165G>T
NM_001278612.1:c.71G>T NP_001265541.1:p.Arg24Ile
NM_004681.3:c.71G>T NP_004672.2:p.Arg24Ile
NM_004681.4:c.71G>T MANE Select NP_004672.2:p.Arg24Ile
NM_001278612.2:c.71G>T NP_001265541.1:p.Arg24Ile
Search 100 bp 5'
Search 100 bp 3'