Canonical Allele Identifier: CA2674453135
Gene: RASGRF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206917del , CM000667.2:g.81206917del GRCh38
NC_000005.9:g.80502736del , CM000667.1:g.80502736del GRCh37
NC_000005.8:g.80538492del NCBI36
NG_030334.1:g.251229del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2967+12del MANE Select ENSP00000265080.4:n.2967+12del
ENST00000265080.8:c.2967+12del ENSP00000265080.4:n.2967+12del
ENST00000503795.1:c.2967+12del ENSP00000421771.1:n.2967+12del
NM_006909.2:c.2967+12del NP_008840.1:n.2967+12del
XM_017009682.2:c.2682+12del XP_016865171.1:n.2682+12del
XR_002956166.1:n.3083+12del
NM_006909.3:c.2967+12del MANE Select NP_008840.1:n.2967+12del