Canonical Allele Identifier: CA385490069

Gene: MARS1 ARHGAP9

Linked Data

• ClinVar Variation Id: 1965121
• ClinVar RCV Id: RCV002726566
• dbSNP Id: rs1875589608
• MyVariant Identifiers: chr12:g.57881946A>G (hg19) ; chr12:g.57488163A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57488163A>G , CM000674.2:g.57488163A>G	GRCh38
NC_000012.11:g.57881946A>G , CM000674.1:g.57881946A>G	GRCh37
NC_000012.10:g.56168213A>G	NCBI36
NG_034077.1:g.5211A>G
NG_023205.2:g.5652T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.73A>G (MARS1) MANE Select	ENSP00000262027.5:p.Arg25Gly
ENST00000393797.7:c.-204+449T>C (ARHGAP9)	ENSP00000377386.3:n.-204+449T>C
ENST00000550288.6:c.-274+449T>C (ARHGAP9)	ENSP00000473445.2:n.-274+449T>C
ENST00000262027.9:c.73A>G (MARS1)	ENSP00000262027.5:p.Arg25Gly
ENST00000393797.6:c.10+449T>C (ARHGAP9)	ENSP00000377386.2:n.10+449T>C
ENST00000447721.6:n.96A>G (MARS1)
ENST00000537638.6:c.73A>G (MARS1)	ENSP00000446168.2:p.Arg25Gly
ENST00000545888.6:c.73A>G (MARS1)	ENSP00000439307.2:p.Arg25Gly
ENST00000546481.1:n.102A>G (MARS1)
ENST00000547062.5:n.96A>G (MARS1)
ENST00000547501.5:c.73A>G (MARS1)	ENSP00000447145.1:p.Arg25Gly
ENST00000548674.5:n.79+61A>G (MARS1)
ENST00000548714.5:n.96A>G (MARS1)
ENST00000549074.5:c.73A>G (MARS1)	ENSP00000447258.1:p.Arg25Gly
ENST00000550288.5:c.-37+449T>C (ARHGAP9)	ENSP00000473445.1:n.-37+449T>C
ENST00000550449.5:n.108A>G (MARS1)
ENST00000551431.5:c.73A>G (MARS1)	ENSP00000446729.1:p.Arg25Gly
ENST00000551842.5:n.96A>G (MARS1)
ENST00000551892.1:c.73A>G (MARS1)	ENSP00000450018.1:p.Arg25Gly
ENST00000552007.5:c.73A>G (MARS1)	ENSP00000448576.1:p.Arg25Gly
ENST00000553162.5:n.96A>G (MARS1)
ENST00000628866.2:c.73A>G (MARS1)	ENSP00000486738.1:p.Arg25Gly
ENST00000630571.2:c.73A>G (MARS1)	ENSP00000485951.1:p.Arg25Gly
ENST00000630803.1:c.73A>G (MARS1)	ENSP00000486356.1:p.Arg25Gly
NM_004990.3:c.73A>G (MARS1)	NP_004981.2:p.Arg25Gly
XM_006719398.2:c.-554A>G (MARS1)	XP_006719461.1:n.-554A>G
XM_011538353.1:c.73A>G (MARS1)	XP_011536655.1:p.Arg25Gly
NM_001319850.1:c.10+449T>C (ARHGAP9)	NP_001306779.1:n.10+449T>C
XM_006719398.4:c.-554A>G (MARS1)	XP_006719461.1:n.-554A>G
XR_001748704.2:n.96A>G (MARS1)
XR_002957327.1:n.96A>G (MARS1)
NM_001319850.2:c.-204+449T>C (ARHGAP9)	NP_001306779.2:n.-204+449T>C
NM_004990.4:c.73A>G (MARS1) MANE Select	NP_004981.2:p.Arg25Gly