Canonical Allele Identifier: CA2614978357

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722115-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722115C>A , CM000673.2:g.72722115C>A	GRCh38
NC_000011.9:g.72433160C>A , CM000673.1:g.72433160C>A	GRCh37
NC_000011.8:g.72110808C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4505G>T MANE Select	ENSP00000377233.3:n.509+4505G>T
ENST00000334211.12:c.-492G>T	ENSP00000335506.8:n.-492G>T
ENST00000359373.9:c.509+4505G>T	ENSP00000352332.5:n.509+4505G>T
ENST00000393609.7:c.509+4505G>T	ENSP00000377233.3:n.509+4505G>T
NM_001040118.2:c.509+4505G>T	NP_001035207.1:n.509+4505G>T
NM_001135190.1:c.-492G>T	NP_001128662.1:n.-492G>T
NM_015242.4:c.-492G>T	NP_056057.2:n.-492G>T
NM_001369489.1:c.-492G>T	NP_001356418.1:n.-492G>T
NR_161388.1:n.226G>T
NM_001040118.3:c.509+4505G>T MANE Select	NP_001035207.1:n.509+4505G>T
NM_001135190.2:c.-492G>T	NP_001128662.1:n.-492G>T
NM_015242.5:c.-492G>T	NP_056057.2:n.-492G>T