Canonical Allele Identifier: CA337491932
Gene: EIF1AY HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.20591193A>C
GRCh37 chrY:g.22753079A>C
gnomAD v3:
Y:20591193 A / C
gnomAD v4:
chrY-20591193-A-C
Joint Max Group AF 0.02948009 (SAS)
Genomes Max Group AF 0.02948009 (SAS)
dbSNP:
13447442
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20591193A>C , CM000686.2:g.20591193A>C GRCh38
NC_000024.9:g.22753079A>C , CM000686.1:g.22753079A>C GRCh37
NC_000024.8:g.21162467A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361365.7:c.430-1148A>C MANE Select ENSP00000354722.2:n.430-1148A>C
ENST00000361365.6:c.430-1148A>C ENSP00000354722.2:n.430-1148A>C
ENST00000382772.3:c.379-1148A>C ENSP00000372222.3:n.379-1148A>C
ENST00000464196.5:n.2859-1148A>C
ENST00000485584.1:n.352-1148A>C
NM_001278612.1:c.379-1148A>C NP_001265541.1:n.379-1148A>C
NM_004681.3:c.430-1148A>C NP_004672.2:n.430-1148A>C
NM_004681.4:c.430-1148A>C MANE Select NP_004672.2:n.430-1148A>C
NM_001278612.2:c.379-1148A>C NP_001265541.1:n.379-1148A>C
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