Canonical Allele Identifier: CA814488205
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs1370695140
MyVariant Identifiers: chr5:g.80502622_80502623insT (hg19) chr5:g.81206803_81206804insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206804dup , CM000667.2:g.81206804dup GRCh38
NC_000005.9:g.80502623dup , CM000667.1:g.80502623dup GRCh37
NC_000005.8:g.80538379dup NCBI36
NG_030334.1:g.251116dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2907-41dup MANE Select ENSP00000265080.4:n.2907-41dup
ENST00000265080.8:c.2907-41dup ENSP00000265080.4:n.2907-41dup
ENST00000503795.1:c.2907-41dup ENSP00000421771.1:n.2907-41dup
NM_006909.2:c.2907-41dup NP_008840.1:n.2907-41dup
XM_017009682.2:c.2622-41dup XP_016865171.1:n.2622-41dup
XR_002956166.1:n.3023-41dup
NM_006909.3:c.2907-41dup MANE Select NP_008840.1:n.2907-41dup
Search 100 bp 5'
Search 100 bp 3'