Canonical Allele Identifier: CA406404827
Gene: RSPH6A HGNC NCBI

Linked Data

dbSNP Id: rs1489026799

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45804377C>T , CM000681.2:g.45804377C>T GRCh38
NC_000019.9:g.46307635C>T , CM000681.1:g.46307635C>T GRCh37
NC_000019.8:g.50999475C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221538.8:c.1528G>A MANE Select ENSP00000221538.2:p.Glu510Lys
ENST00000221538.7:c.1528G>A ENSP00000221538.2:p.Glu510Lys
ENST00000597055.1:c.1528G>A ENSP00000472630.1:p.Glu510Lys
ENST00000600188.5:c.736G>A ENSP00000471559.1:p.Glu246Lys
NM_030785.3:c.1528G>A NP_110412.1:p.Glu510Lys
XM_011527351.1:c.1528G>A XP_011525653.1:p.Glu510Lys
XM_011527351.2:c.1528G>A XP_011525653.1:p.Glu510Lys
NM_030785.4:c.1528G>A MANE Select NP_110412.1:p.Glu510Lys