Canonical Allele Identifier: CA679994323

Gene: ARAP1

Linked Data

• dbSNP Id: rs1171475695
• gnomAD v3: 11-72722097-G-A
• gnomAD v4: 11-72722097-G-A
• MyVariant Identifiers: chr11:g.72433142G>A (hg19) ; chr11:g.72722097G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722097G>A , CM000673.2:g.72722097G>A	GRCh38
NC_000011.9:g.72433142G>A , CM000673.1:g.72433142G>A	GRCh37
NC_000011.8:g.72110790G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393609.8:c.509+4523C>T MANE Select	ENSP00000377233.3:n.509+4523C>T
ENST00000334211.12:c.-474C>T	ENSP00000335506.8:n.-474C>T
ENST00000359373.9:c.509+4523C>T	ENSP00000352332.5:n.509+4523C>T
ENST00000393609.7:c.509+4523C>T	ENSP00000377233.3:n.509+4523C>T
NM_001040118.2:c.509+4523C>T	NP_001035207.1:n.509+4523C>T
NM_001135190.1:c.-474C>T	NP_001128662.1:n.-474C>T
NM_015242.4:c.-474C>T	NP_056057.2:n.-474C>T
NM_001369489.1:c.-474C>T	NP_001356418.1:n.-474C>T
NR_161388.1:n.244C>T
NM_001040118.3:c.509+4523C>T MANE Select	NP_001035207.1:n.509+4523C>T
NM_001135190.2:c.-474C>T	NP_001128662.1:n.-474C>T
NM_015242.5:c.-474C>T	NP_056057.2:n.-474C>T