Canonical Allele Identifier: CA2674453311
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81207303-C-CAGAT
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207304_81207307dup , CM000667.2:g.81207304_81207307dup GRCh38
NC_000005.9:g.80503123_80503126dup , CM000667.1:g.80503123_80503126dup GRCh37
NC_000005.8:g.80538879_80538882dup NCBI36
NG_030334.1:g.251616_251619dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.3026_3029dup MANE Select ENSP00000265080.4:p.Thr1011AspfsTer27
ENST00000265080.8:c.3026_3029dup ENSP00000265080.4:p.Thr1011AspfsTer27
ENST00000503795.1:c.3026_3029dup ENSP00000421771.1:p.Thr1011AspfsTer27
NM_006909.2:c.3026_3029dup NP_008840.1:p.Thr1011AspfsTer27
XM_017009682.2:c.2741_2744dup XP_016865171.1:p.Thr916AspfsTer27
XR_002956166.1:n.3142_3145dup
NM_006909.3:c.3026_3029dup MANE Select NP_008840.1:p.Thr1011AspfsTer27
Search 100 bp 5'
Search 100 bp 3'