Canonical Allele Identifier: CA414947526
Gene: RPS4Y1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2734904A>C (hg19) chrY:g.2866863A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866863A>C , CM000686.2:g.2866863A>C GRCh38
NC_000024.9:g.2734904A>C , CM000686.1:g.2734904A>C GRCh37
NC_000024.8:g.2794904A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.761A>C MANE Select ENSP00000250784.7:p.Lys254Thr
ENST00000250784.12:c.761A>C ENSP00000250784.7:p.Lys254Thr
ENST00000477725.1:n.905A>C
ENST00000515575.1:n.42+12092A>C
NM_001008.3:c.761A>C NP_000999.1:p.Lys254Thr
NM_001008.4:c.761A>C MANE Select NP_000999.1:p.Lys254Thr
Search 100 bp 5'
Search 100 bp 3'