Canonical Allele Identifier: CA414854910
Gene: EIF1AY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22741568G>C (hg19) chrY:g.20579682G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20579682G>C , CM000686.2:g.20579682G>C GRCh38
NC_000024.9:g.22741568G>C , CM000686.1:g.22741568G>C GRCh37
NC_000024.8:g.21150956G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361365.7:c.91G>C MANE Select ENSP00000354722.2:p.Asp31His
ENST00000361365.6:c.91G>C ENSP00000354722.2:p.Asp31His
ENST00000382772.3:c.91G>C ENSP00000372222.3:p.Asp31His
ENST00000465253.1:n.185G>C
NM_001278612.1:c.91G>C NP_001265541.1:p.Asp31His
NM_004681.3:c.91G>C NP_004672.2:p.Asp31His
NM_004681.4:c.91G>C MANE Select NP_004672.2:p.Asp31His
NM_001278612.2:c.91G>C NP_001265541.1:p.Asp31His
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