Canonical Allele Identifier: CA2674453129
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81206846-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206849del , CM000667.2:g.81206849del GRCh38
NC_000005.9:g.80502668del , CM000667.1:g.80502668del GRCh37
NC_000005.8:g.80538424del NCBI36
NG_030334.1:g.251161del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2911del MANE Select ENSP00000265080.4:p.Leu971PhefsTer11
ENST00000265080.8:c.2911del ENSP00000265080.4:p.Leu971PhefsTer11
ENST00000503795.1:c.2911del ENSP00000421771.1:p.Leu971PhefsTer11
NM_006909.2:c.2911del NP_008840.1:p.Leu971PhefsTer11
XM_017009682.2:c.2626del XP_016865171.1:p.Leu876PhefsTer11
XR_002956166.1:n.3027del
NM_006909.3:c.2911del MANE Select NP_008840.1:p.Leu971PhefsTer11
Search 100 bp 5'
Search 100 bp 3'