Canonical Allele Identifier: CA625314482

Gene: RAI1

Linked Data

• gnomAD v2: 17-17697094-CA-C
• gnomAD v4: 17-17793780-CA-C
• MyVariant Identifiers: chr17:g.17697095del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793781del , CM000679.2:g.17793781del	GRCh38
NC_000017.10:g.17697095del , CM000679.1:g.17697095del	GRCh37
NC_000017.9:g.17637820del	NCBI36
NG_007101.2:g.117309del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.833del MANE Select	ENSP00000323074.4:p.Gln278ArgfsTer?
ENST00000640861.1:c.767del	ENSP00000491773.1:p.Gln256ArgfsTer?
ENST00000353383.5:c.833del	ENSP00000323074.4:p.Gln278ArgfsTer?
ENST00000395774.1:c.833del	ENSP00000379120.1:p.Gln278ArgfsTer?
NM_030665.3:c.833del	NP_109590.3:p.Gln278ArgfsTer?
XM_017024025.1:c.833del	XP_016879514.1:p.Gln278ArgfsTer?
XM_017024026.1:c.833del	XP_016879515.1:p.Gln278ArgfsTer?
XM_017024027.1:c.833del	XP_016879516.1:p.Gln278ArgfsTer?
XM_017024028.2:c.833del	XP_016879517.1:p.Gln278ArgfsTer?
NM_030665.4:c.833del MANE Select	NP_109590.3:p.Gln278ArgfsTer?