Canonical Allele Identifier: CA715983731

Gene: RASGRF1

Linked Data

• dbSNP Id: rs1487225717
• MyVariant Identifiers: chr15:g.79273948A>G (hg19) ; chr15:g.78981606A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78981606A>G , CM000677.2:g.78981606A>G	GRCh38
NC_000015.9:g.79273948A>G , CM000677.1:g.79273948A>G	GRCh37
NC_000015.8:g.77061003A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000558480.7:c.3415-907T>C MANE Select	ENSP00000452781.2:n.3415-907T>C
ENST00000394745.3:c.1111-907T>C	ENSP00000378228.3:n.1111-907T>C
ENST00000419573.7:c.3463-907T>C	ENSP00000405963.3:n.3463-907T>C
ENST00000558480.6:c.3415-907T>C	ENSP00000452781.2:n.3415-907T>C
ENST00000560286.1:n.305-907T>C
ENST00000560334.5:n.3285-907T>C
ENST00000560943.5:n.620-907T>C
ENST00000623620.1:n.61T>C
NM_001145648.1:c.3415-907T>C	NP_001139120.1:n.3415-907T>C
NM_002891.4:c.3463-907T>C	NP_002882.3:n.3463-907T>C
NM_153815.2:c.1111-907T>C	NP_722522.1:n.1111-907T>C
XM_005254578.3:c.3415-907T>C	XP_005254635.1:n.3415-907T>C
XM_011521863.1:c.3463-907T>C	XP_011520165.1:n.3463-907T>C
XM_011521864.1:c.3454-907T>C	XP_011520166.1:n.3454-907T>C
XM_011521865.1:c.3424-907T>C	XP_011520167.1:n.3424-907T>C
XM_011521866.1:c.3463-907T>C	XP_011520168.1:n.3463-907T>C
XM_011521867.1:c.3463-907T>C	XP_011520169.1:n.3463-907T>C
NR_148998.1:n.435+2283A>G
XM_011521866.3:c.3463-907T>C	XP_011520168.1:n.3463-907T>C
XM_011521867.3:c.3463-907T>C	XP_011520169.1:n.3463-907T>C
XM_017022455.2:c.3454-907T>C	XP_016877944.1:n.3454-907T>C
XM_017022456.2:c.3424-907T>C	XP_016877945.1:n.3424-907T>C
XM_017022457.2:c.3424-907T>C	XP_016877946.1:n.3424-907T>C
XM_017022458.2:c.3415-907T>C	XP_016877947.1:n.3415-907T>C
XM_017022459.2:c.3424-907T>C	XP_016877948.1:n.3424-907T>C
NM_001145648.2:c.3415-907T>C	NP_001139120.1:n.3415-907T>C
NM_002891.5:c.3463-907T>C	NP_002882.3:n.3463-907T>C
NM_001145648.3:c.3415-907T>C MANE Select	NP_001139120.1:n.3415-907T>C
NM_002891.6:c.3463-907T>C	NP_002882.3:n.3463-907T>C
NM_153815.3:c.1111-907T>C	NP_722522.1:n.1111-907T>C