Canonical Allele Identifier: CA16043575

Gene: GPRASP1 ARMCX5-GPRASP2

Linked Data

• ClinVar Variation Id: 373909
• ClinVar RCV Id: RCV000415157
• dbSNP Id: rs1057518762
• MyVariant Identifiers: chrX:g.101912220G>C (hg19) ; chrX:g.102657292G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.102657292G>C , CM000685.2:g.102657292G>C	GRCh38
NC_000023.10:g.101912220G>C , CM000685.1:g.101912220G>C	GRCh37
NC_000023.9:g.101798876G>C	NCBI36
NG_021332.1:g.10927G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537097.2:c.3379G>C (GPRASP1) MANE Select	ENSP00000445683.1:p.Glu1127Gln
ENST00000652542.1:c.3379G>C (GPRASP1)	ENSP00000498934.1:p.Glu1127Gln
ENST00000361600.9:c.3379G>C (GPRASP1)	ENSP00000355146.4:p.Glu1127Gln
ENST00000415986.5:c.3379G>C (GPRASP1)	ENSP00000393691.1:p.Glu1127Gln
ENST00000444152.5:c.3379G>C (GPRASP1)	ENSP00000409420.1:p.Glu1127Gln
ENST00000537097.1:c.3379G>C (GPRASP1)	ENSP00000445683.1:p.Glu1127Gln
NM_001099410.1:c.3379G>C (GPRASP1)	NP_001092880.1:p.Glu1127Gln
NM_001099411.1:c.3379G>C (GPRASP1)	NP_001092881.1:p.Glu1127Gln
NM_001184727.1:c.3379G>C (GPRASP1)	NP_001171656.1:p.Glu1127Gln
NM_001199818.1:c.-480+51639G>C (ARMCX5-GPRASP2)	NP_001186747.1:n.-480+51639G>C
NM_014710.4:c.3379G>C (GPRASP1)	NP_055525.3:p.Glu1127Gln
NM_001350268.1:c.-966+51639G>C (ARMCX5-GPRASP2)	NP_001337197.1:n.-966+51639G>C
NR_146584.1:n.666+51639G>C (ARMCX5-GPRASP2)
NM_001184727.2:c.3379G>C (GPRASP1) MANE Select	NP_001171656.1:p.Glu1127Gln
NM_001350268.2:c.-966+51639G>C (ARMCX5-GPRASP2)	NP_001337197.1:n.-966+51639G>C
NM_014710.5:c.3379G>C (GPRASP1)	NP_055525.3:p.Glu1127Gln
NR_146584.2:n.649+51639G>C (ARMCX5-GPRASP2)
NM_001099410.2:c.3379G>C (GPRASP1)	NP_001092880.1:p.Glu1127Gln
NM_001099411.2:c.3379G>C (GPRASP1)	NP_001092881.1:p.Glu1127Gln
NR_146584.3:n.649+51639G>C (ARMCX5-GPRASP2)