Canonical Allele Identifier: CA2674453240
Gene: RASGRF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207129_81207132del , CM000667.2:g.81207129_81207132del GRCh38
NC_000005.9:g.80502948_80502951del , CM000667.1:g.80502948_80502951del GRCh37
NC_000005.8:g.80538704_80538707del NCBI36
NG_030334.1:g.251441_251444del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2968-117_2968-114del MANE Select ENSP00000265080.4:n.2968-117_2968-114del
ENST00000265080.8:c.2968-117_2968-114del ENSP00000265080.4:n.2968-117_2968-114del
ENST00000503795.1:c.2968-117_2968-114del ENSP00000421771.1:n.2968-117_2968-114del
NM_006909.2:c.2968-117_2968-114del NP_008840.1:n.2968-117_2968-114del
XM_017009682.2:c.2683-117_2683-114del XP_016865171.1:n.2683-117_2683-114del
XR_002956166.1:n.3084-117_3084-114del
NM_006909.3:c.2968-117_2968-114del MANE Select NP_008840.1:n.2968-117_2968-114del