Canonical Allele Identifier: CA406404845
Gene: RSPH6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45804386C>G , CM000681.2:g.45804386C>G GRCh38
NC_000019.9:g.46307644C>G , CM000681.1:g.46307644C>G GRCh37
NC_000019.8:g.50999484C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221538.8:c.1519G>C MANE Select ENSP00000221538.2:p.Gly507Arg
ENST00000221538.7:c.1519G>C ENSP00000221538.2:p.Gly507Arg
ENST00000597055.1:c.1519G>C ENSP00000472630.1:p.Gly507Arg
ENST00000600188.5:c.727G>C ENSP00000471559.1:p.Gly243Arg
NM_030785.3:c.1519G>C NP_110412.1:p.Gly507Arg
XM_011527351.1:c.1519G>C XP_011525653.1:p.Gly507Arg
XM_011527351.2:c.1519G>C XP_011525653.1:p.Gly507Arg
NM_030785.4:c.1519G>C MANE Select NP_110412.1:p.Gly507Arg