Canonical Allele Identifier: CA2614978618

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722185-G-GAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722186_72722187insTA , CM000673.2:g.72722186_72722187insTA	GRCh38
NC_000011.9:g.72433231_72433232insTA , CM000673.1:g.72433231_72433232insTA	GRCh37
NC_000011.8:g.72110879_72110880insTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4434_509+4435insAT MANE Select	ENSP00000377233.3:n.509+4434_509+4435insAT
ENST00000334211.12:c.-563_-562insAT	ENSP00000335506.8:n.-563_-562insAT
ENST00000359373.9:c.509+4434_509+4435insAT	ENSP00000352332.5:n.509+4434_509+4435insAT
ENST00000393609.7:c.509+4434_509+4435insAT	ENSP00000377233.3:n.509+4434_509+4435insAT
NM_001040118.2:c.509+4434_509+4435insAT	NP_001035207.1:n.509+4434_509+4435insAT
NM_001135190.1:c.-563_-562insAT	NP_001128662.1:n.-563_-562insAT
NM_015242.4:c.-563_-562insAT	NP_056057.2:n.-563_-562insAT
NM_001369489.1:c.-563_-562insAT	NP_001356418.1:n.-563_-562insAT
NR_161388.1:n.155_156insAT
NM_001040118.3:c.509+4434_509+4435insAT MANE Select	NP_001035207.1:n.509+4434_509+4435insAT
NM_001135190.2:c.-563_-562insAT	NP_001128662.1:n.-563_-562insAT
NM_015242.5:c.-563_-562insAT	NP_056057.2:n.-563_-562insAT