Canonical Allele Identifier: CA2338615008
Gene: RSPH6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45804381G= , CM000681.2:g.45804381G= GRCh38
NC_000019.9:g.46307639G= , CM000681.1:g.46307639G= GRCh37
NC_000019.8:g.50999479G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221538.8:c.1524C= MANE Select ENSP00000221538.2:p.Asp508=
ENST00000221538.7:c.1524C= ENSP00000221538.2:p.Asp508=
ENST00000597055.1:c.1524C= ENSP00000472630.1:p.Asp508=
ENST00000600188.5:c.732C= ENSP00000471559.1:p.Asp244=
NM_030785.3:c.1524C= NP_110412.1:p.Asp508=
XM_011527351.1:c.1524C= XP_011525653.1:p.Asp508=
XM_011527351.2:c.1524C= XP_011525653.1:p.Asp508=
NM_030785.4:c.1524C= MANE Select NP_110412.1:p.Asp508=