Canonical Allele Identifier: CA2674453195

Gene: RASGRF2

Linked Data

• gnomAD v4: 5-81207033-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81207036_81207037del , CM000667.2:g.81207036_81207037del	GRCh38
NC_000005.9:g.80502855_80502856del , CM000667.1:g.80502855_80502856del	GRCh37
NC_000005.8:g.80538611_80538612del	NCBI36
NG_030334.1:g.251348_251349del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265080.9:c.2967+131_2967+132del MANE Select	ENSP00000265080.4:n.2967+131_2967+132del
ENST00000265080.8:c.2967+131_2967+132del	ENSP00000265080.4:n.2967+131_2967+132del
ENST00000503795.1:c.2967+131_2967+132del	ENSP00000421771.1:n.2967+131_2967+132del
NM_006909.2:c.2967+131_2967+132del	NP_008840.1:n.2967+131_2967+132del
XM_017009682.2:c.2682+131_2682+132del	XP_016865171.1:n.2682+131_2682+132del
XR_002956166.1:n.3083+131_3083+132del
NM_006909.3:c.2967+131_2967+132del MANE Select	NP_008840.1:n.2967+131_2967+132del