Canonical Allele Identifier: CA2614978678

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722196-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722197_72722198insGG , CM000673.2:g.72722197_72722198insGG	GRCh38
NC_000011.9:g.72433242_72433243insGG , CM000673.1:g.72433242_72433243insGG	GRCh37
NC_000011.8:g.72110890_72110891insGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4423_509+4424insCC MANE Select	ENSP00000377233.3:n.509+4423_509+4424insCC
ENST00000334211.12:c.-574_-573insCC	ENSP00000335506.8:n.-574_-573insCC
ENST00000359373.9:c.509+4423_509+4424insCC	ENSP00000352332.5:n.509+4423_509+4424insCC
ENST00000393609.7:c.509+4423_509+4424insCC	ENSP00000377233.3:n.509+4423_509+4424insCC
NM_001040118.2:c.509+4423_509+4424insCC	NP_001035207.1:n.509+4423_509+4424insCC
NM_001135190.1:c.-574_-573insCC	NP_001128662.1:n.-574_-573insCC
NM_015242.4:c.-574_-573insCC	NP_056057.2:n.-574_-573insCC
NM_001369489.1:c.-574_-573insCC	NP_001356418.1:n.-574_-573insCC
NR_161388.1:n.144_145insCC
NM_001040118.3:c.509+4423_509+4424insCC MANE Select	NP_001035207.1:n.509+4423_509+4424insCC
NM_001135190.2:c.-574_-573insCC	NP_001128662.1:n.-574_-573insCC
NM_015242.5:c.-574_-573insCC	NP_056057.2:n.-574_-573insCC