Canonical Allele Identifier: CA520170305
Gene: EIF1AY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22741547A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20579661A>C , CM000686.2:g.20579661A>C GRCh38
NC_000024.9:g.22741547A>C , CM000686.1:g.22741547A>C GRCh37
NC_000024.8:g.21150935A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361365.7:c.70A>C MANE Select ENSP00000354722.2:p.Arg24=
ENST00000361365.6:c.70A>C ENSP00000354722.2:p.Arg24=
ENST00000382772.3:c.70A>C ENSP00000372222.3:p.Arg24=
ENST00000465253.1:n.164A>C
NM_001278612.1:c.70A>C NP_001265541.1:p.Arg24=
NM_004681.3:c.70A>C NP_004672.2:p.Arg24=
NM_004681.4:c.70A>C MANE Select NP_004672.2:p.Arg24=
NM_001278612.2:c.70A>C NP_001265541.1:p.Arg24=