Canonical Allele Identifier: CA2614980433

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72712977-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712977A>G , CM000673.2:g.72712977A>G	GRCh38
NC_000011.9:g.72424022A>G , CM000673.1:g.72424022A>G	GRCh37
NC_000011.8:g.72101670A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393609.8:c.747+199T>C MANE Select	ENSP00000377233.3:n.747+199T>C
ENST00000334211.12:c.12+199T>C	ENSP00000335506.8:n.12+199T>C
ENST00000359373.9:c.747+199T>C	ENSP00000352332.5:n.747+199T>C
ENST00000393605.7:c.-382T>C	ENSP00000377230.3:n.-382T>C
ENST00000393609.7:c.747+199T>C	ENSP00000377233.3:n.747+199T>C
ENST00000426523.5:c.12+199T>C	ENSP00000392264.1:n.12+199T>C
ENST00000429686.5:c.12+199T>C	ENSP00000403127.1:n.12+199T>C
ENST00000465814.5:n.676T>C
NM_001040118.2:c.747+199T>C	NP_001035207.1:n.747+199T>C
NM_001135190.1:c.12+199T>C	NP_001128662.1:n.12+199T>C
NM_015242.4:c.12+199T>C	NP_056057.2:n.12+199T>C
NM_001369489.1:c.12+199T>C	NP_001356418.1:n.12+199T>C
NR_161388.1:n.729+199T>C
NM_001040118.3:c.747+199T>C MANE Select	NP_001035207.1:n.747+199T>C
NM_001135190.2:c.12+199T>C	NP_001128662.1:n.12+199T>C
NM_015242.5:c.12+199T>C	NP_056057.2:n.12+199T>C