Canonical Allele Identifier: CA224453144

Gene: ARAP1

Linked Data

• dbSNP Id: rs386374137
• MyVariant Identifiers: chr11:g.72433237_72433238insAG (hg19) ; chr11:g.72722192_72722193insAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722192_72722193insAG , CM000673.2:g.72722192_72722193insAG	GRCh38
NC_000011.9:g.72433237_72433238insAG , CM000673.1:g.72433237_72433238insAG	GRCh37
NC_000011.8:g.72110885_72110886insAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4427_509+4428insCT MANE Select	ENSP00000377233.3:n.509+4427_509+4428insCT
ENST00000334211.12:c.-570_-569insCT	ENSP00000335506.8:n.-570_-569insCT
ENST00000359373.9:c.509+4427_509+4428insCT	ENSP00000352332.5:n.509+4427_509+4428insCT
ENST00000393609.7:c.509+4427_509+4428insCT	ENSP00000377233.3:n.509+4427_509+4428insCT
NM_001040118.2:c.509+4427_509+4428insCT	NP_001035207.1:n.509+4427_509+4428insCT
NM_001135190.1:c.-570_-569insCT	NP_001128662.1:n.-570_-569insCT
NM_015242.4:c.-570_-569insCT	NP_056057.2:n.-570_-569insCT
NM_001369489.1:c.-570_-569insCT	NP_001356418.1:n.-570_-569insCT
NR_161388.1:n.148_149insCT
NM_001040118.3:c.509+4427_509+4428insCT MANE Select	NP_001035207.1:n.509+4427_509+4428insCT
NM_001135190.2:c.-570_-569insCT	NP_001128662.1:n.-570_-569insCT
NM_015242.5:c.-570_-569insCT	NP_056057.2:n.-570_-569insCT