Canonical Allele Identifier: CA224448320

Gene: ARAP1

Linked Data

• dbSNP Id: rs1023995268
• gnomAD v4: 11-72712912-A-T
• MyVariant Identifiers: chr11:g.72423957A>T (hg19) ; chr11:g.72712912A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712912A>T , CM000673.2:g.72712912A>T	GRCh38
NC_000011.9:g.72423957A>T , CM000673.1:g.72423957A>T	GRCh37
NC_000011.8:g.72101605A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393609.8:c.747+264T>A MANE Select	ENSP00000377233.3:n.747+264T>A
ENST00000334211.12:c.12+264T>A	ENSP00000335506.8:n.12+264T>A
ENST00000359373.9:c.747+264T>A	ENSP00000352332.5:n.747+264T>A
ENST00000393605.7:c.-317T>A	ENSP00000377230.3:n.-317T>A
ENST00000393609.7:c.747+264T>A	ENSP00000377233.3:n.747+264T>A
ENST00000426523.5:c.12+264T>A	ENSP00000392264.1:n.12+264T>A
ENST00000429686.5:c.12+264T>A	ENSP00000403127.1:n.12+264T>A
ENST00000465814.5:n.741T>A
NM_001040118.2:c.747+264T>A	NP_001035207.1:n.747+264T>A
NM_001135190.1:c.12+264T>A	NP_001128662.1:n.12+264T>A
NM_015242.4:c.12+264T>A	NP_056057.2:n.12+264T>A
NM_001369489.1:c.12+264T>A	NP_001356418.1:n.12+264T>A
NR_161388.1:n.729+264T>A
NM_001040118.3:c.747+264T>A MANE Select	NP_001035207.1:n.747+264T>A
NM_001135190.2:c.12+264T>A	NP_001128662.1:n.12+264T>A
NM_015242.5:c.12+264T>A	NP_056057.2:n.12+264T>A