Canonical Allele Identifier: CA406404864
Gene: RSPH6A HGNC NCBI

Linked Data

dbSNP Id: rs1162826166

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45804394T>C , CM000681.2:g.45804394T>C GRCh38
NC_000019.9:g.46307652T>C , CM000681.1:g.46307652T>C GRCh37
NC_000019.8:g.50999492T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221538.8:c.1511A>G MANE Select ENSP00000221538.2:p.Glu504Gly
ENST00000221538.7:c.1511A>G ENSP00000221538.2:p.Glu504Gly
ENST00000597055.1:c.1511A>G ENSP00000472630.1:p.Glu504Gly
ENST00000600188.5:c.719A>G ENSP00000471559.1:p.Glu240Gly
NM_030785.3:c.1511A>G NP_110412.1:p.Glu504Gly
XM_011527351.1:c.1511A>G XP_011525653.1:p.Glu504Gly
XM_011527351.2:c.1511A>G XP_011525653.1:p.Glu504Gly
NM_030785.4:c.1511A>G MANE Select NP_110412.1:p.Glu504Gly