Canonical Allele Identifier: CA519439302
Gene: RPS4Y1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2734845T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866804T>C , CM000686.2:g.2866804T>C GRCh38
NC_000024.9:g.2734845T>C , CM000686.1:g.2734845T>C GRCh37
NC_000024.8:g.2794845T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.702T>C MANE Select ENSP00000250784.7:p.Pro234=
ENST00000250784.12:c.702T>C ENSP00000250784.7:p.Pro234=
ENST00000430575.1:c.729T>C ENSP00000415317.1:p.Pro243=
ENST00000477725.1:n.846T>C
ENST00000515575.1:n.42+12033T>C
NM_001008.3:c.702T>C NP_000999.1:p.Pro234=
NM_001008.4:c.702T>C MANE Select NP_000999.1:p.Pro234=