Canonical Allele Identifier: CA1558747273
Gene: RASGRF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207205_81207207delinsCCT , CM000667.2:g.81207205_81207207delinsCCT GRCh38
NC_000005.9:g.80503024_80503026delinsCCT , CM000667.1:g.80503024_80503026delinsCCT GRCh37
NC_000005.8:g.80538780_80538782delinsCCT NCBI36
NG_030334.1:g.251517_251519delinsCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2968-41_2968-39delinsCCT MANE Select ENSP00000265080.4:n.2968-41_2968-39delinsCCT
ENST00000265080.8:c.2968-41_2968-39delinsCCT ENSP00000265080.4:n.2968-41_2968-39delinsCCT
ENST00000503795.1:c.2968-41_2968-39delinsCCT ENSP00000421771.1:n.2968-41_2968-39delinsCCT
NM_006909.2:c.2968-41_2968-39delinsCCT NP_008840.1:n.2968-41_2968-39delinsCCT
XM_017009682.2:c.2683-41_2683-39delinsCCT XP_016865171.1:n.2683-41_2683-39delinsCCT
XR_002956166.1:n.3084-41_3084-39delinsCCT
NM_006909.3:c.2968-41_2968-39delinsCCT MANE Select NP_008840.1:n.2968-41_2968-39delinsCCT