Canonical Allele Identifier: CA2674453190
Gene: RASGRF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207025_81207027del , CM000667.2:g.81207025_81207027del GRCh38
NC_000005.9:g.80502844_80502846del , CM000667.1:g.80502844_80502846del GRCh37
NC_000005.8:g.80538600_80538602del NCBI36
NG_030334.1:g.251337_251339del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2967+120_2967+122del MANE Select ENSP00000265080.4:n.2967+120_2967+122del
ENST00000265080.8:c.2967+120_2967+122del ENSP00000265080.4:n.2967+120_2967+122del
ENST00000503795.1:c.2967+120_2967+122del ENSP00000421771.1:n.2967+120_2967+122del
NM_006909.2:c.2967+120_2967+122del NP_008840.1:n.2967+120_2967+122del
XM_017009682.2:c.2682+120_2682+122del XP_016865171.1:n.2682+120_2682+122del
XR_002956166.1:n.3083+120_3083+122del
NM_006909.3:c.2967+120_2967+122del MANE Select NP_008840.1:n.2967+120_2967+122del