Canonical Allele Identifier: CA224453133

Gene: ARAP1

Linked Data

• dbSNP Id: rs2306611
• MyVariant Identifiers: chr11:g.72433220G>C (hg19) ; chr11:g.72722175G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722175G>C , CM000673.2:g.72722175G>C	GRCh38
NC_000011.9:g.72433220G>C , CM000673.1:g.72433220G>C	GRCh37
NC_000011.8:g.72110868G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4445C>G MANE Select	ENSP00000377233.3:n.509+4445C>G
ENST00000334211.12:c.-552C>G	ENSP00000335506.8:n.-552C>G
ENST00000359373.9:c.509+4445C>G	ENSP00000352332.5:n.509+4445C>G
ENST00000393609.7:c.509+4445C>G	ENSP00000377233.3:n.509+4445C>G
NM_001040118.2:c.509+4445C>G	NP_001035207.1:n.509+4445C>G
NM_001135190.1:c.-552C>G	NP_001128662.1:n.-552C>G
NM_015242.4:c.-552C>G	NP_056057.2:n.-552C>G
NM_001369489.1:c.-552C>G	NP_001356418.1:n.-552C>G
NR_161388.1:n.166C>G
NM_001040118.3:c.509+4445C>G MANE Select	NP_001035207.1:n.509+4445C>G
NM_001135190.2:c.-552C>G	NP_001128662.1:n.-552C>G
NM_015242.5:c.-552C>G	NP_056057.2:n.-552C>G