Canonical Allele Identifier: CA2674453091
Gene: RASGRF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206743_81206744del , CM000667.2:g.81206743_81206744del GRCh38
NC_000005.9:g.80502562_80502563del , CM000667.1:g.80502562_80502563del GRCh37
NC_000005.8:g.80538318_80538319del NCBI36
NG_030334.1:g.251055_251056del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2907-102_2907-101del MANE Select ENSP00000265080.4:n.2907-102_2907-101del
ENST00000265080.8:c.2907-102_2907-101del ENSP00000265080.4:n.2907-102_2907-101del
ENST00000503795.1:c.2907-102_2907-101del ENSP00000421771.1:n.2907-102_2907-101del
NM_006909.2:c.2907-102_2907-101del NP_008840.1:n.2907-102_2907-101del
XM_017009682.2:c.2622-102_2622-101del XP_016865171.1:n.2622-102_2622-101del
XR_002956166.1:n.3023-102_3023-101del
NM_006909.3:c.2907-102_2907-101del MANE Select NP_008840.1:n.2907-102_2907-101del