Canonical Allele Identifier: CA912999130

Gene: RAI1

Linked Data

• MyVariant Identifiers: chr17:g.17697132_17697133insCAGCAACAGCAG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793820_17793821insGCAACAGCAGCA , CM000679.2:g.17793820_17793821insGCAACAGCAGCA	GRCh38
NC_000017.10:g.17697134_17697135insGCAACAGCAGCA , CM000679.1:g.17697134_17697135insGCAACAGCAGCA	GRCh37
NC_000017.9:g.17637859_17637860insGCAACAGCAGCA	NCBI36
NG_007101.2:g.117348_117349insGCAACAGCAGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.872_873insGCAACAGCAGCA MANE Select	ENSP00000323074.4:p.Gln291_Ala292insGlnGlnGlnGln
ENST00000640861.1:c.806_807insGCAACAGCAGCA	ENSP00000491773.1:p.Gln269_Ala270insGlnGlnGlnGln
ENST00000353383.5:c.872_873insGCAACAGCAGCA	ENSP00000323074.4:p.Gln291_Ala292insGlnGlnGlnGln
ENST00000395774.1:c.872_873insGCAACAGCAGCA	ENSP00000379120.1:p.Gln291_Ala292insGlnGlnGlnGln
NM_030665.3:c.872_873insGCAACAGCAGCA	NP_109590.3:p.Gln291_Ala292insGlnGlnGlnGln
XM_017024025.1:c.872_873insGCAACAGCAGCA	XP_016879514.1:p.Gln291_Ala292insGlnGlnGlnGln
XM_017024026.1:c.872_873insGCAACAGCAGCA	XP_016879515.1:p.Gln291_Ala292insGlnGlnGlnGln
XM_017024027.1:c.872_873insGCAACAGCAGCA	XP_016879516.1:p.Gln291_Ala292insGlnGlnGlnGln
XM_017024028.2:c.872_873insGCAACAGCAGCA	XP_016879517.1:p.Gln291_Ala292insGlnGlnGlnGln
NM_030665.4:c.872_873insGCAACAGCAGCA MANE Select	NP_109590.3:p.Gln291_Ala292insGlnGlnGlnGln