Canonical Allele Identifier: CA498422780

Gene: RAI1

Linked Data

• gnomAD v4: 17-17793516-A-C
• MyVariant Identifiers: chr17:g.17696830A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793516A>C , CM000679.2:g.17793516A>C	GRCh38
NC_000017.10:g.17696830A>C , CM000679.1:g.17696830A>C	GRCh37
NC_000017.9:g.17637555A>C	NCBI36
NG_007101.2:g.117044A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.568A>C MANE Select	ENSP00000323074.4:p.Arg190=
ENST00000640861.1:c.568A>C	ENSP00000491773.1:p.Arg190=
ENST00000353383.5:c.568A>C	ENSP00000323074.4:p.Arg190=
ENST00000395774.1:c.568A>C	ENSP00000379120.1:p.Arg190=
NM_030665.3:c.568A>C	NP_109590.3:p.Arg190=
XM_017024025.1:c.568A>C	XP_016879514.1:p.Arg190=
XM_017024026.1:c.568A>C	XP_016879515.1:p.Arg190=
XM_017024027.1:c.568A>C	XP_016879516.1:p.Arg190=
XM_017024028.2:c.568A>C	XP_016879517.1:p.Arg190=
NM_030665.4:c.568A>C MANE Select	NP_109590.3:p.Arg190=