Canonical Allele Identifier: CA121319201

Gene: RASGRF2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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