Canonical Allele Identifier: CA2674453254
Gene: RASGRF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207146_81207147insAAA , CM000667.2:g.81207146_81207147insAAA GRCh38
NC_000005.9:g.80502965_80502966insAAA , CM000667.1:g.80502965_80502966insAAA GRCh37
NC_000005.8:g.80538721_80538722insAAA NCBI36
NG_030334.1:g.251458_251459insAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2968-100_2968-99insAAA MANE Select ENSP00000265080.4:n.2968-100_2968-99insAAA
ENST00000265080.8:c.2968-100_2968-99insAAA ENSP00000265080.4:n.2968-100_2968-99insAAA
ENST00000503795.1:c.2968-100_2968-99insAAA ENSP00000421771.1:n.2968-100_2968-99insAAA
NM_006909.2:c.2968-100_2968-99insAAA NP_008840.1:n.2968-100_2968-99insAAA
XM_017009682.2:c.2683-100_2683-99insAAA XP_016865171.1:n.2683-100_2683-99insAAA
XR_002956166.1:n.3084-100_3084-99insAAA
NM_006909.3:c.2968-100_2968-99insAAA MANE Select NP_008840.1:n.2968-100_2968-99insAAA