Canonical Allele Identifier: CA2574916164
Gene: ARAP1 HGNC NCBI

Linked Data

gnomAD v4: 11-72721997-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72721997G>T , CM000673.2:g.72721997G>T GRCh38
NC_000011.9:g.72433042G>T , CM000673.1:g.72433042G>T GRCh37
NC_000011.8:g.72110690G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393609.8:c.509+4623C>A MANE Select ENSP00000377233.3:n.509+4623C>A
ENST00000334211.12:c.-374C>A ENSP00000335506.8:n.-374C>A
ENST00000359373.9:c.509+4623C>A ENSP00000352332.5:n.509+4623C>A
ENST00000393609.7:c.509+4623C>A ENSP00000377233.3:n.509+4623C>A
ENST00000426523.5:c.-374C>A ENSP00000392264.1:n.-374C>A
ENST00000429686.5:c.-374C>A ENSP00000403127.1:n.-374C>A
ENST00000465814.5:n.92C>A
NM_001040118.2:c.509+4623C>A NP_001035207.1:n.509+4623C>A
NM_001135190.1:c.-374C>A NP_001128662.1:n.-374C>A
NM_015242.4:c.-374C>A NP_056057.2:n.-374C>A
NM_001369489.1:c.-374C>A NP_001356418.1:n.-374C>A
NR_161388.1:n.344C>A
NM_001040118.3:c.509+4623C>A MANE Select NP_001035207.1:n.509+4623C>A
NM_001135190.2:c.-374C>A NP_001128662.1:n.-374C>A
NM_015242.5:c.-374C>A NP_056057.2:n.-374C>A
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