Canonical Allele Identifier: CA23896582

Gene: RAVER2

Linked Data

• dbSNP Id: rs34314637
• MyVariant Identifiers: chr1:g.65298886_65298887insG (hg19) ; chr1:g.64833203_64833204insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.64833203_64833204insG , CM000663.2:g.64833203_64833204insG	GRCh38
NC_000001.10:g.65298886_65298887insG , CM000663.1:g.65298886_65298887insG	GRCh37
NC_000001.9:g.65071474_65071475insG	NCBI36
NG_023402.1:g.138301_138302insC
NG_023402.2:g.239543_239544insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000294428.8:c.*2218_*2219insG MANE Select	ENSP00000294428.3:n.*2218_*2219insG
ENST00000294428.7:c.*2218_*2219insG	ENSP00000294428.3:n.*2218_*2219insG
ENST00000371072.8:c.*2218_*2219insG	ENSP00000360112.4:n.*2218_*2219insG
NM_018211.3:c.*2218_*2219insG	NP_060681.2:n.*2218_*2219insG
XM_006710738.2:c.*2218_*2219insG	XP_006710801.2:n.*2218_*2219insG
NM_001366165.1:c.*2218_*2219insG	NP_001353094.1:n.*2218_*2219insG
XR_946693.3:n.4637_4638insG
NM_018211.4:c.*2218_*2219insG	NP_060681.2:n.*2218_*2219insG
NM_001366165.2:c.*2218_*2219insG MANE Select	NP_001353094.1:n.*2218_*2219insG