Canonical Allele Identifier: CA381770443

Gene: ARAP1

Linked Data

• MyVariant Identifiers: chr11:g.72423487G>T (hg19) ; chr11:g.72712442G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712442G>T , CM000673.2:g.72712442G>T	GRCh38
NC_000011.9:g.72423487G>T , CM000673.1:g.72423487G>T	GRCh37
NC_000011.8:g.72101135G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.874C>A MANE Select	ENSP00000377233.3:p.Pro292Thr
ENST00000334211.12:c.139C>A	ENSP00000335506.8:p.Pro47Thr
ENST00000359373.9:c.874C>A	ENSP00000352332.5:p.Pro292Thr
ENST00000393605.7:c.154C>A	ENSP00000377230.3:p.Pro52Thr
ENST00000393609.7:c.874C>A	ENSP00000377233.3:p.Pro292Thr
ENST00000426523.5:c.139C>A	ENSP00000392264.1:p.Pro47Thr
ENST00000429686.5:c.139C>A	ENSP00000403127.1:p.Pro47Thr
ENST00000465814.5:n.1211C>A
NM_001040118.2:c.874C>A	NP_001035207.1:p.Pro292Thr
NM_001135190.1:c.139C>A	NP_001128662.1:p.Pro47Thr
NM_015242.4:c.139C>A	NP_056057.2:p.Pro47Thr
NM_001369489.1:c.139C>A	NP_001356418.1:p.Pro47Thr
NR_161388.1:n.856C>A
NM_001040118.3:c.874C>A MANE Select	NP_001035207.1:p.Pro292Thr
NM_001135190.2:c.139C>A	NP_001128662.1:p.Pro47Thr
NM_015242.5:c.139C>A	NP_056057.2:p.Pro47Thr