Canonical Allele Identifier: CA2189768945

Gene: RASGRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78981731C= , CM000677.2:g.78981731C=	GRCh38
NC_000015.9:g.79274073C= , CM000677.1:g.79274073C=	GRCh37
NC_000015.8:g.77061128C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000558480.7:c.3415-1032G= MANE Select	ENSP00000452781.2:n.3415-1032G=
ENST00000394745.3:c.1111-1032G=	ENSP00000378228.3:n.1111-1032G=
ENST00000419573.7:c.3463-1032G=	ENSP00000405963.3:n.3463-1032G=
ENST00000558480.6:c.3415-1032G=	ENSP00000452781.2:n.3415-1032G=
ENST00000560286.1:n.305-1032G=
ENST00000560334.5:n.3285-1032G=
ENST00000560943.5:n.620-1032G=
NM_001145648.1:c.3415-1032G=	NP_001139120.1:n.3415-1032G=
NM_002891.4:c.3463-1032G=	NP_002882.3:n.3463-1032G=
NM_153815.2:c.1111-1032G=	NP_722522.1:n.1111-1032G=
XM_005254578.3:c.3415-1032G=	XP_005254635.1:n.3415-1032G=
XM_011521863.1:c.3463-1032G=	XP_011520165.1:n.3463-1032G=
XM_011521864.1:c.3454-1032G=	XP_011520166.1:n.3454-1032G=
XM_011521865.1:c.3424-1032G=	XP_011520167.1:n.3424-1032G=
XM_011521866.1:c.3463-1032G=	XP_011520168.1:n.3463-1032G=
XM_011521867.1:c.3463-1032G=	XP_011520169.1:n.3463-1032G=
NR_148998.1:n.435+2408C=
XM_011521866.3:c.3463-1032G=	XP_011520168.1:n.3463-1032G=
XM_011521867.3:c.3463-1032G=	XP_011520169.1:n.3463-1032G=
XM_017022455.2:c.3454-1032G=	XP_016877944.1:n.3454-1032G=
XM_017022456.2:c.3424-1032G=	XP_016877945.1:n.3424-1032G=
XM_017022457.2:c.3424-1032G=	XP_016877946.1:n.3424-1032G=
XM_017022458.2:c.3415-1032G=	XP_016877947.1:n.3415-1032G=
XM_017022459.2:c.3424-1032G=	XP_016877948.1:n.3424-1032G=
NM_001145648.2:c.3415-1032G=	NP_001139120.1:n.3415-1032G=
NM_002891.5:c.3463-1032G=	NP_002882.3:n.3463-1032G=
NM_001145648.3:c.3415-1032G= MANE Select	NP_001139120.1:n.3415-1032G=
NM_002891.6:c.3463-1032G=	NP_002882.3:n.3463-1032G=
NM_153815.3:c.1111-1032G=	NP_722522.1:n.1111-1032G=