Canonical Allele Identifier: CA381770817

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72712552-C-G
• MyVariant Identifiers: chr11:g.72423597C>G (hg19) ; chr11:g.72712552C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712552C>G , CM000673.2:g.72712552C>G	GRCh38
NC_000011.9:g.72423597C>G , CM000673.1:g.72423597C>G	GRCh37
NC_000011.8:g.72101245C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.764G>C MANE Select	ENSP00000377233.3:p.Ser255Thr
ENST00000334211.12:c.29G>C	ENSP00000335506.8:p.Ser10Thr
ENST00000359373.9:c.764G>C	ENSP00000352332.5:p.Ser255Thr
ENST00000393605.7:c.44G>C	ENSP00000377230.3:p.Ser15Thr
ENST00000393609.7:c.764G>C	ENSP00000377233.3:p.Ser255Thr
ENST00000426523.5:c.29G>C	ENSP00000392264.1:p.Ser10Thr
ENST00000429686.5:c.29G>C	ENSP00000403127.1:p.Ser10Thr
ENST00000465814.5:n.1101G>C
NM_001040118.2:c.764G>C	NP_001035207.1:p.Ser255Thr
NM_001135190.1:c.29G>C	NP_001128662.1:p.Ser10Thr
NM_015242.4:c.29G>C	NP_056057.2:p.Ser10Thr
NM_001369489.1:c.29G>C	NP_001356418.1:p.Ser10Thr
NR_161388.1:n.746G>C
NM_001040118.3:c.764G>C MANE Select	NP_001035207.1:p.Ser255Thr
NM_001135190.2:c.29G>C	NP_001128662.1:p.Ser10Thr
NM_015242.5:c.29G>C	NP_056057.2:p.Ser10Thr