Canonical Allele Identifier: CA414854863
Gene: EIF1AY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22741557T>G (hg19) chrY:g.20579671T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20579671T>G , CM000686.2:g.20579671T>G GRCh38
NC_000024.9:g.22741557T>G , CM000686.1:g.22741557T>G GRCh37
NC_000024.8:g.21150945T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361365.7:c.80T>G MANE Select ENSP00000354722.2:p.Val27Gly
ENST00000361365.6:c.80T>G ENSP00000354722.2:p.Val27Gly
ENST00000382772.3:c.80T>G ENSP00000372222.3:p.Val27Gly
ENST00000465253.1:n.174T>G
NM_001278612.1:c.80T>G NP_001265541.1:p.Val27Gly
NM_004681.3:c.80T>G NP_004672.2:p.Val27Gly
NM_004681.4:c.80T>G MANE Select NP_004672.2:p.Val27Gly
NM_001278612.2:c.80T>G NP_001265541.1:p.Val27Gly
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