Canonical Allele Identifier: CA3760478
Gene: ITPR3 HGNC NCBI

Linked Data

dbSNP Id: rs748085345
gnomAD v2: 6-33636884-G-A
gnomAD v3: 6-33669107-G-A
gnomAD v4: 6-33669107-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33669107G>A , CM000668.2:g.33669107G>A GRCh38
NC_000006.11:g.33636884G>A , CM000668.1:g.33636884G>A GRCh37
NC_000006.10:g.33744862G>A NCBI36
NG_027729.1:g.52729G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000605930.3:c.2140G>A MANE Select ENSP00000475177.1:p.Glu714Lys
ENST00000374316.9:c.2140G>A ENSP00000363435.4:p.Glu714Lys
ENST00000605930.2:c.2140G>A ENSP00000475177.1:p.Glu714Lys
NM_002224.3:c.2140G>A NP_002215.2:p.Glu714Lys
XM_011514576.1:c.2209G>A XP_011512878.1:p.Glu737Lys
XM_011514577.1:c.1957G>A XP_011512879.1:p.Glu653Lys
XM_011514577.3:c.1957G>A XP_011512879.1:p.Glu653Lys
XM_017010832.1:c.2140G>A XP_016866321.1:p.Glu714Lys
NM_002224.4:c.2140G>A MANE Select NP_002215.2:p.Glu714Lys