Canonical Allele Identifier: CA2338615019

Gene: RSPH6A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45804402C= , CM000681.2:g.45804402C=	GRCh38
NC_000019.9:g.46307660C= , CM000681.1:g.46307660C=	GRCh37
NC_000019.8:g.50999500C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221538.8:c.1503G= MANE Select	ENSP00000221538.2:p.Gln501=
ENST00000221538.7:c.1503G=	ENSP00000221538.2:p.Gln501=
ENST00000597055.1:c.1503G=	ENSP00000472630.1:p.Gln501=
ENST00000600188.5:c.711G=	ENSP00000471559.1:p.Gln237=
NM_030785.3:c.1503G=	NP_110412.1:p.Gln501=
XM_011527351.1:c.1503G=	XP_011525653.1:p.Gln501=
XM_011527351.2:c.1503G=	XP_011525653.1:p.Gln501=
NM_030785.4:c.1503G= MANE Select	NP_110412.1:p.Gln501=