Canonical Allele Identifier: CA23896530

Gene: RAVER2

Linked Data

• dbSNP Id: rs1553157345
• MyVariant Identifiers: chr1:g.65298776_65298777insTTA (hg19) ; chr1:g.64833093_64833094insTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.64833095_64833096insATT , CM000663.2:g.64833095_64833096insATT	GRCh38
NC_000001.10:g.65298778_65298779insATT , CM000663.1:g.65298778_65298779insATT	GRCh37
NC_000001.9:g.65071366_65071367insATT	NCBI36
NG_023402.1:g.138411_138412insTAA
NG_023402.2:g.239653_239654insTAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000294428.8:c.*2110_*2111insATT MANE Select	ENSP00000294428.3:n.*2110_*2111insATT
ENST00000294428.7:c.*2110_*2111insATT	ENSP00000294428.3:n.*2110_*2111insATT
ENST00000371072.8:c.*2110_*2111insATT	ENSP00000360112.4:n.*2110_*2111insATT
NM_018211.3:c.*2110_*2111insATT	NP_060681.2:n.*2110_*2111insATT
XM_006710738.2:c.*2110_*2111insATT	XP_006710801.2:n.*2110_*2111insATT
NM_001366165.1:c.*2110_*2111insATT	NP_001353094.1:n.*2110_*2111insATT
XR_946693.3:n.4529_4530insATT
NM_018211.4:c.*2110_*2111insATT	NP_060681.2:n.*2110_*2111insATT
NM_001366165.2:c.*2110_*2111insATT MANE Select	NP_001353094.1:n.*2110_*2111insATT