Canonical Allele Identifier: CA679988573

Gene: ARAP1

Linked Data

• dbSNP Id: rs1205134805
• gnomAD v4: 11-72712419-AGGGTGGCCGGACACTCACTT-A
• MyVariant Identifiers: chr11:g.72423465_72423484del (hg19) ; chr11:g.72712420_72712439del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712423_72712442del , CM000673.2:g.72712423_72712442del	GRCh38
NC_000011.9:g.72423468_72423487del , CM000673.1:g.72423468_72423487del	GRCh37
NC_000011.8:g.72101116_72101135del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.877_878+18del
ENST00000334211.12:c.142_143+18del
ENST00000359373.9:c.877_878+18del
ENST00000393605.7:c.157_158+18del
ENST00000393609.7:c.877_878+18del
ENST00000426523.5:c.142_143+18del
ENST00000429686.5:c.142_143+18del
ENST00000465814.5:n.1214_1215+18del
NM_001040118.2:c.877_878+18del
NM_001135190.1:c.142_143+18del
NM_015242.4:c.142_143+18del
NM_001369489.1:c.142_143+18del
NR_161388.1:n.859_860+18del
NM_001040118.3:c.877_878+18del
NM_001135190.2:c.142_143+18del
NM_015242.5:c.142_143+18del