Canonical Allele Identifier: CA2614977992
Gene: ARAP1 HGNC NCBI

Linked Data

gnomAD v4: 11-72721962-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72721962G>T , CM000673.2:g.72721962G>T GRCh38
NC_000011.9:g.72433007G>T , CM000673.1:g.72433007G>T GRCh37
NC_000011.8:g.72110655G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393609.8:c.509+4658C>A MANE Select ENSP00000377233.3:n.509+4658C>A
ENST00000334211.12:c.-339C>A ENSP00000335506.8:n.-339C>A
ENST00000359373.9:c.509+4658C>A ENSP00000352332.5:n.509+4658C>A
ENST00000393609.7:c.509+4658C>A ENSP00000377233.3:n.509+4658C>A
ENST00000426523.5:c.-339C>A ENSP00000392264.1:n.-339C>A
ENST00000429686.5:c.-339C>A ENSP00000403127.1:n.-339C>A
ENST00000465814.5:n.127C>A
NM_001040118.2:c.509+4658C>A NP_001035207.1:n.509+4658C>A
NM_001135190.1:c.-339C>A NP_001128662.1:n.-339C>A
NM_015242.4:c.-339C>A NP_056057.2:n.-339C>A
NM_001369489.1:c.-339C>A NP_001356418.1:n.-339C>A
NR_161388.1:n.379C>A
NM_001040118.3:c.509+4658C>A MANE Select NP_001035207.1:n.509+4658C>A
NM_001135190.2:c.-339C>A NP_001128662.1:n.-339C>A
NM_015242.5:c.-339C>A NP_056057.2:n.-339C>A
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