Canonical Allele Identifier: CA1982116772

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72721973_72721974delinsCA , CM000673.2:g.72721973_72721974delinsCA	GRCh38
NC_000011.9:g.72433018_72433019delinsCA , CM000673.1:g.72433018_72433019delinsCA	GRCh37
NC_000011.8:g.72110666_72110667delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4646_509+4647delinsTG MANE Select	ENSP00000377233.3:n.509+4646_509+4647delinsTG
ENST00000334211.12:c.-351_-350delinsTG	ENSP00000335506.8:n.-351_-350delinsTG
ENST00000359373.9:c.509+4646_509+4647delinsTG	ENSP00000352332.5:n.509+4646_509+4647delinsTG
ENST00000393609.7:c.509+4646_509+4647delinsTG	ENSP00000377233.3:n.509+4646_509+4647delinsTG
ENST00000426523.5:c.-351_-350delinsTG	ENSP00000392264.1:n.-351_-350delinsTG
ENST00000429686.5:c.-351_-350delinsTG	ENSP00000403127.1:n.-351_-350delinsTG
ENST00000465814.5:n.115_116delinsTG
NM_001040118.2:c.509+4646_509+4647delinsTG	NP_001035207.1:n.509+4646_509+4647delinsTG
NM_001135190.1:c.-351_-350delinsTG	NP_001128662.1:n.-351_-350delinsTG
NM_015242.4:c.-351_-350delinsTG	NP_056057.2:n.-351_-350delinsTG
NM_001369489.1:c.-351_-350delinsTG	NP_001356418.1:n.-351_-350delinsTG
NR_161388.1:n.367_368delinsTG
NM_001040118.3:c.509+4646_509+4647delinsTG MANE Select	NP_001035207.1:n.509+4646_509+4647delinsTG
NM_001135190.2:c.-351_-350delinsTG	NP_001128662.1:n.-351_-350delinsTG
NM_015242.5:c.-351_-350delinsTG	NP_056057.2:n.-351_-350delinsTG