Canonical Allele Identifier: CA10571326
Gene: RPS4Y1 HGNC NCBI

Linked Data

dbSNP Id: rs748727264
ExAC: Y:2734808 T / TA
gnomAD v2: Y-2734808-T-TA
MyVariant Identifiers: chrY:g.2734808_2734809insA (hg19) chrY:g.2866767_2866768insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866768dup , CM000686.2:g.2866768dup GRCh38
NC_000024.9:g.2734809dup , CM000686.1:g.2734809dup GRCh37
NC_000024.8:g.2794809dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000250784.13:c.691-25dup MANE Select ENSP00000250784.7:n.691-25dup
ENST00000250784.12:c.691-25dup ENSP00000250784.7:n.691-25dup
ENST00000430575.1:c.718-25dup ENSP00000415317.1:n.718-25dup
ENST00000477725.1:n.835-25dup
ENST00000515575.1:n.42+11997dup
NM_001008.3:c.691-25dup NP_000999.1:n.691-25dup
NM_001008.4:c.691-25dup MANE Select NP_000999.1:n.691-25dup
Search 100 bp 5'
Search 100 bp 3'