Canonical Allele Identifier: CA2674453176

Gene: RASGRF2

Linked Data

• gnomAD v4: 5-81207009-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81207009_81207010insA , CM000667.2:g.81207009_81207010insA	GRCh38
NC_000005.9:g.80502828_80502829insA , CM000667.1:g.80502828_80502829insA	GRCh37
NC_000005.8:g.80538584_80538585insA	NCBI36
NG_030334.1:g.251321_251322insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265080.9:c.2967+104_2967+105insA MANE Select	ENSP00000265080.4:n.2967+104_2967+105insA
ENST00000265080.8:c.2967+104_2967+105insA	ENSP00000265080.4:n.2967+104_2967+105insA
ENST00000503795.1:c.2967+104_2967+105insA	ENSP00000421771.1:n.2967+104_2967+105insA
NM_006909.2:c.2967+104_2967+105insA	NP_008840.1:n.2967+104_2967+105insA
XM_017009682.2:c.2682+104_2682+105insA	XP_016865171.1:n.2682+104_2682+105insA
XR_002956166.1:n.3083+104_3083+105insA
NM_006909.3:c.2967+104_2967+105insA MANE Select	NP_008840.1:n.2967+104_2967+105insA