Canonical Allele Identifier: CA475638152

Gene: ARAP1

Linked Data

• MyVariant Identifiers: chr11:g.72423524C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712479C>A , CM000673.2:g.72712479C>A	GRCh38
NC_000011.9:g.72423524C>A , CM000673.1:g.72423524C>A	GRCh37
NC_000011.8:g.72101172C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.837G>T MANE Select	ENSP00000377233.3:p.Gly279=
ENST00000334211.12:c.102G>T	ENSP00000335506.8:p.Gly34=
ENST00000359373.9:c.837G>T	ENSP00000352332.5:p.Gly279=
ENST00000393605.7:c.117G>T	ENSP00000377230.3:p.Gly39=
ENST00000393609.7:c.837G>T	ENSP00000377233.3:p.Gly279=
ENST00000426523.5:c.102G>T	ENSP00000392264.1:p.Gly34=
ENST00000429686.5:c.102G>T	ENSP00000403127.1:p.Gly34=
ENST00000465814.5:n.1174G>T
NM_001040118.2:c.837G>T	NP_001035207.1:p.Gly279=
NM_001135190.1:c.102G>T	NP_001128662.1:p.Gly34=
NM_015242.4:c.102G>T	NP_056057.2:p.Gly34=
NM_001369489.1:c.102G>T	NP_001356418.1:p.Gly34=
NR_161388.1:n.819G>T
NM_001040118.3:c.837G>T MANE Select	NP_001035207.1:p.Gly279=
NM_001135190.2:c.102G>T	NP_001128662.1:p.Gly34=
NM_015242.5:c.102G>T	NP_056057.2:p.Gly34=