Canonical Allele Identifier: CA406404927
Gene: RSPH6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45804421C>G , CM000681.2:g.45804421C>G GRCh38
NC_000019.9:g.46307679C>G , CM000681.1:g.46307679C>G GRCh37
NC_000019.8:g.50999519C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221538.8:c.1484G>C MANE Select ENSP00000221538.2:p.Ser495Thr
ENST00000221538.7:c.1484G>C ENSP00000221538.2:p.Ser495Thr
ENST00000597055.1:c.1484G>C ENSP00000472630.1:p.Ser495Thr
ENST00000600188.5:c.692G>C ENSP00000471559.1:p.Ser231Thr
NM_030785.3:c.1484G>C NP_110412.1:p.Ser495Thr
XM_011527351.1:c.1484G>C XP_011525653.1:p.Ser495Thr
XM_011527351.2:c.1484G>C XP_011525653.1:p.Ser495Thr
NM_030785.4:c.1484G>C MANE Select NP_110412.1:p.Ser495Thr