Canonical Allele Identifier: CA2674453228
Gene: RASGRF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207115_81207116insAGCT , CM000667.2:g.81207115_81207116insAGCT GRCh38
NC_000005.9:g.80502934_80502935insAGCT , CM000667.1:g.80502934_80502935insAGCT GRCh37
NC_000005.8:g.80538690_80538691insAGCT NCBI36
NG_030334.1:g.251427_251428insAGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.2968-131_2968-130insAGCT MANE Select ENSP00000265080.4:n.2968-131_2968-130insA...
ENST00000265080.8:c.2968-131_2968-130insAGCT ENSP00000265080.4:n.2968-131_2968-130insA...
ENST00000503795.1:c.2968-131_2968-130insAGCT ENSP00000421771.1:n.2968-131_2968-130insA...
NM_006909.2:c.2968-131_2968-130insAGCT NP_008840.1:n.2968-131_2968-130insAGCT
XM_017009682.2:c.2683-131_2683-130insAGCT XP_016865171.1:n.2683-131_2683-130insAGCT...
XR_002956166.1:n.3084-131_3084-130insAGCT
NM_006909.3:c.2968-131_2968-130insAGCT MANE Select NP_008840.1:n.2968-131_2968-130insAGCT