Canonical Allele Identifier: CA406404948
Gene: RSPH6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45804431T>G , CM000681.2:g.45804431T>G GRCh38
NC_000019.9:g.46307689T>G , CM000681.1:g.46307689T>G GRCh37
NC_000019.8:g.50999529T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221538.8:c.1474A>C MANE Select ENSP00000221538.2:p.Thr492Pro
ENST00000221538.7:c.1474A>C ENSP00000221538.2:p.Thr492Pro
ENST00000597055.1:c.1474A>C ENSP00000472630.1:p.Thr492Pro
ENST00000600188.5:c.682A>C ENSP00000471559.1:p.Thr228Pro
NM_030785.3:c.1474A>C NP_110412.1:p.Thr492Pro
XM_011527351.1:c.1474A>C XP_011525653.1:p.Thr492Pro
XM_011527351.2:c.1474A>C XP_011525653.1:p.Thr492Pro
NM_030785.4:c.1474A>C MANE Select NP_110412.1:p.Thr492Pro