Canonical Allele Identifier: CA2614977882

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72721929-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72721929T>G , CM000673.2:g.72721929T>G	GRCh38
NC_000011.9:g.72432974T>G , CM000673.1:g.72432974T>G	GRCh37
NC_000011.8:g.72110622T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393609.8:c.509+4691A>C MANE Select	ENSP00000377233.3:n.509+4691A>C
ENST00000334211.12:c.-306A>C	ENSP00000335506.8:n.-306A>C
ENST00000359373.9:c.509+4691A>C	ENSP00000352332.5:n.509+4691A>C
ENST00000393609.7:c.509+4691A>C	ENSP00000377233.3:n.509+4691A>C
ENST00000426523.5:c.-306A>C	ENSP00000392264.1:n.-306A>C
ENST00000429686.5:c.-306A>C	ENSP00000403127.1:n.-306A>C
ENST00000465814.5:n.160A>C
NM_001040118.2:c.509+4691A>C	NP_001035207.1:n.509+4691A>C
NM_001135190.1:c.-306A>C	NP_001128662.1:n.-306A>C
NM_015242.4:c.-306A>C	NP_056057.2:n.-306A>C
NM_001369489.1:c.-306A>C	NP_001356418.1:n.-306A>C
NR_161388.1:n.412A>C
NM_001040118.3:c.509+4691A>C MANE Select	NP_001035207.1:n.509+4691A>C
NM_001135190.2:c.-306A>C	NP_001128662.1:n.-306A>C
NM_015242.5:c.-306A>C	NP_056057.2:n.-306A>C