Canonical Allele Identifier: CA414947422
Gene: RPS4Y1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2734877G>T (hg19) chrY:g.2866836G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866836G>T , CM000686.2:g.2866836G>T GRCh38
NC_000024.9:g.2734877G>T , CM000686.1:g.2734877G>T GRCh37
NC_000024.8:g.2794877G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.734G>T MANE Select ENSP00000250784.7:p.Arg245Leu
ENST00000250784.12:c.734G>T ENSP00000250784.7:p.Arg245Leu
ENST00000430575.1:c.761G>T ENSP00000415317.1:p.Arg254Leu
ENST00000477725.1:n.878G>T
ENST00000515575.1:n.42+12065G>T
NM_001008.3:c.734G>T NP_000999.1:p.Arg245Leu
NM_001008.4:c.734G>T MANE Select NP_000999.1:p.Arg245Leu
Search 100 bp 5'
Search 100 bp 3'