Canonical Allele Identifier: CA1139998431

Gene: RAVER2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.64833094_64833100delinsTTTGTTT , CM000663.2:g.64833094_64833100delinsTTTGTTT	GRCh38
NC_000001.10:g.65298777_65298783delinsTTTGTTT , CM000663.1:g.65298777_65298783delinsTTTGTTT	GRCh37
NC_000001.9:g.65071365_65071371delinsTTTGTTT	NCBI36
NG_023402.1:g.138405_138411delinsAAACAAA
NG_023402.2:g.239647_239653delinsAAACAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294428.8:c.*2109_*2115delinsTTTGTTT MANE Select	ENSP00000294428.3:n.*2109_*2115delinsTTTGTTT
ENST00000294428.7:c.*2109_*2115delinsTTTGTTT	ENSP00000294428.3:n.*2109_*2115delinsTTTGTTT
ENST00000371072.8:c.*2109_*2115delinsTTTGTTT	ENSP00000360112.4:n.*2109_*2115delinsTTTGTTT
NM_018211.3:c.*2109_*2115delinsTTTGTTT	NP_060681.2:n.*2109_*2115delinsTTTGTTT
XM_006710738.2:c.*2109_*2115delinsTTTGTTT	XP_006710801.2:n.*2109_*2115delinsTTTGTTT
NM_001366165.1:c.*2109_*2115delinsTTTGTTT	NP_001353094.1:n.*2109_*2115delinsTTTGTTT
XR_946693.3:n.4528_4534delinsTTTGTTT
NM_018211.4:c.*2109_*2115delinsTTTGTTT	NP_060681.2:n.*2109_*2115delinsTTTGTTT
NM_001366165.2:c.*2109_*2115delinsTTTGTTT MANE Select	NP_001353094.1:n.*2109_*2115delinsTTTGTTT