Canonical Allele Identifier: CA381770437

Gene: ARAP1

Linked Data

• dbSNP Id: rs1857063908
• MyVariant Identifiers: chr11:g.72423484T>C (hg19) ; chr11:g.72712439T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712439T>C , CM000673.2:g.72712439T>C	GRCh38
NC_000011.9:g.72423484T>C , CM000673.1:g.72423484T>C	GRCh37
NC_000011.8:g.72101132T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.877A>G MANE Select	ENSP00000377233.3:p.Asn293Asp
ENST00000334211.12:c.142A>G	ENSP00000335506.8:p.Asn48Asp
ENST00000359373.9:c.877A>G	ENSP00000352332.5:p.Asn293Asp
ENST00000393605.7:c.157A>G	ENSP00000377230.3:p.Asn53Asp
ENST00000393609.7:c.877A>G	ENSP00000377233.3:p.Asn293Asp
ENST00000426523.5:c.142A>G	ENSP00000392264.1:p.Asn48Asp
ENST00000429686.5:c.142A>G	ENSP00000403127.1:p.Asn48Asp
ENST00000465814.5:n.1214A>G
NM_001040118.2:c.877A>G	NP_001035207.1:p.Asn293Asp
NM_001135190.1:c.142A>G	NP_001128662.1:p.Asn48Asp
NM_015242.4:c.142A>G	NP_056057.2:p.Asn48Asp
NM_001369489.1:c.142A>G	NP_001356418.1:p.Asn48Asp
NR_161388.1:n.859A>G
NM_001040118.3:c.877A>G MANE Select	NP_001035207.1:p.Asn293Asp
NM_001135190.2:c.142A>G	NP_001128662.1:p.Asn48Asp
NM_015242.5:c.142A>G	NP_056057.2:p.Asn48Asp