Canonical Allele Identifier: CA1558692433
Gene: RASGRF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81069496G= , CM000667.2:g.81069496G= GRCh38
NC_000005.9:g.80365315G= , CM000667.1:g.80365315G= GRCh37
NC_000005.8:g.80401071G= NCBI36
NG_030334.1:g.113808G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.544-996G= MANE Select ENSP00000265080.4:n.544-996G=
ENST00000638442.1:c.544-996G= ENSP00000491428.1:n.544-996G=
ENST00000265080.8:c.544-996G= ENSP00000265080.4:n.544-996G=
ENST00000503795.1:c.544-996G= ENSP00000421771.1:n.544-996G=
ENST00000514946.1:n.435-996G=
NM_006909.2:c.544-996G= NP_008840.1:n.544-996G=
XM_005248565.1:c.544-996G= XP_005248622.1:n.544-996G=
XM_017009682.2:c.259-996G= XP_016865171.1:n.259-996G=
XM_017009683.1:c.544-996G= XP_016865172.1:n.544-996G=
XM_024446141.1:c.544-996G= XP_024301909.1:n.544-996G=
XM_024446142.1:c.544-996G= XP_024301910.1:n.544-996G=
XR_002956166.1:n.611-996G=
NM_006909.3:c.544-996G= MANE Select NP_008840.1:n.544-996G=