Canonical Allele Identifier: CA2338614752

Gene: RSPH6A

Linked Data

• dbSNP Id: rs1600474670

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45803924T>G , CM000681.2:g.45803924T>G	GRCh38
NC_000019.9:g.46307182T>G , CM000681.1:g.46307182T>G	GRCh37
NC_000019.8:g.50999022T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221538.8:c.1653+328A>C MANE Select	ENSP00000221538.2:n.1653+328A>C
ENST00000221538.7:c.1653+328A>C	ENSP00000221538.2:n.1653+328A>C
ENST00000597055.1:c.1653+328A>C	ENSP00000472630.1:n.1653+328A>C
ENST00000600188.5:c.861+328A>C	ENSP00000471559.1:n.861+328A>C
NM_030785.3:c.1653+328A>C	NP_110412.1:n.1653+328A>C
XM_011527351.1:c.1653+328A>C	XP_011525653.1:n.1653+328A>C
XM_011527351.2:c.1653+328A>C	XP_011525653.1:n.1653+328A>C
NM_030785.4:c.1653+328A>C MANE Select	NP_110412.1:n.1653+328A>C