Canonical Allele Identifier: CA2338614758
Gene: RSPH6A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45803930T= , CM000681.2:g.45803930T= GRCh38
NC_000019.9:g.46307188T= , CM000681.1:g.46307188T= GRCh37
NC_000019.8:g.50999028T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221538.8:c.1653+322A= MANE Select ENSP00000221538.2:n.1653+322A=
ENST00000221538.7:c.1653+322A= ENSP00000221538.2:n.1653+322A=
ENST00000597055.1:c.1653+322A= ENSP00000472630.1:n.1653+322A=
ENST00000600188.5:c.861+322A= ENSP00000471559.1:n.861+322A=
NM_030785.3:c.1653+322A= NP_110412.1:n.1653+322A=
XM_011527351.1:c.1653+322A= XP_011525653.1:n.1653+322A=
XM_011527351.2:c.1653+322A= XP_011525653.1:n.1653+322A=
NM_030785.4:c.1653+322A= MANE Select NP_110412.1:n.1653+322A=
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