Canonical Allele Identifier: CA449882610

Gene: ITPR3

Linked Data

• MyVariant Identifiers: chr6:g.33636808A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33669031A>C , CM000668.2:g.33669031A>C	GRCh38
NC_000006.11:g.33636808A>C , CM000668.1:g.33636808A>C	GRCh37
NC_000006.10:g.33744786A>C	NCBI36
NG_027729.1:g.52653A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000605930.3:c.2064A>C MANE Select	ENSP00000475177.1:p.Ser688=
ENST00000374316.9:c.2064A>C	ENSP00000363435.4:p.Ser688=
ENST00000605930.2:c.2064A>C	ENSP00000475177.1:p.Ser688=
NM_002224.3:c.2064A>C	NP_002215.2:p.Ser688=
XM_011514576.1:c.2133A>C	XP_011512878.1:p.Ser711=
XM_011514577.1:c.1881A>C	XP_011512879.1:p.Ser627=
XM_011514577.3:c.1881A>C	XP_011512879.1:p.Ser627=
XM_017010832.1:c.2064A>C	XP_016866321.1:p.Ser688=
NM_002224.4:c.2064A>C MANE Select	NP_002215.2:p.Ser688=