Canonical Allele Identifier: CA507965530

Gene: RSPH6A

Linked Data

• MyVariant Identifiers: chr19:g.46307702G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45804444G>A , CM000681.2:g.45804444G>A	GRCh38
NC_000019.9:g.46307702G>A , CM000681.1:g.46307702G>A	GRCh37
NC_000019.8:g.50999542G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221538.8:c.1461C>T MANE Select	ENSP00000221538.2:p.Arg487=
ENST00000221538.7:c.1461C>T	ENSP00000221538.2:p.Arg487=
ENST00000597055.1:c.1461C>T	ENSP00000472630.1:p.Arg487=
ENST00000600188.5:c.669C>T	ENSP00000471559.1:p.Arg223=
NM_030785.3:c.1461C>T	NP_110412.1:p.Arg487=
XM_011527351.1:c.1461C>T	XP_011525653.1:p.Arg487=
XM_011527351.2:c.1461C>T	XP_011525653.1:p.Arg487=
NM_030785.4:c.1461C>T MANE Select	NP_110412.1:p.Arg487=