Canonical Allele Identifier: CA414854787
Gene: EIF1AY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22741544A>T (hg19) chrY:g.20579658A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20579658A>T , CM000686.2:g.20579658A>T GRCh38
NC_000024.9:g.22741544A>T , CM000686.1:g.22741544A>T GRCh37
NC_000024.8:g.21150932A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361365.7:c.67A>T MANE Select ENSP00000354722.2:p.Lys23Ter
ENST00000361365.6:c.67A>T ENSP00000354722.2:p.Lys23Ter
ENST00000382772.3:c.67A>T ENSP00000372222.3:p.Lys23Ter
ENST00000465253.1:n.161A>T
NM_001278612.1:c.67A>T NP_001265541.1:p.Lys23Ter
NM_004681.3:c.67A>T NP_004672.2:p.Lys23Ter
NM_004681.4:c.67A>T MANE Select NP_004672.2:p.Lys23Ter
NM_001278612.2:c.67A>T NP_001265541.1:p.Lys23Ter
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