Canonical Allele Identifier: CA2338614989
Gene: RSPH6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45804354G= , CM000681.2:g.45804354G= GRCh38
NC_000019.9:g.46307612G= , CM000681.1:g.46307612G= GRCh37
NC_000019.8:g.50999452G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221538.8:c.1551C= MANE Select ENSP00000221538.2:p.Arg517=
ENST00000221538.7:c.1551C= ENSP00000221538.2:p.Arg517=
ENST00000597055.1:c.1551C= ENSP00000472630.1:p.Arg517=
ENST00000600188.5:c.759C= ENSP00000471559.1:p.Arg253=
NM_030785.3:c.1551C= NP_110412.1:p.Arg517=
XM_011527351.1:c.1551C= XP_011525653.1:p.Arg517=
XM_011527351.2:c.1551C= XP_011525653.1:p.Arg517=
NM_030785.4:c.1551C= MANE Select NP_110412.1:p.Arg517=