Canonical Allele Identifier: CA679989137

Gene: ARAP1

Linked Data

• dbSNP Id: rs1187671485
• gnomAD v3: 11-72712775-G-A
• gnomAD v4: 11-72712775-G-A
• MyVariant Identifiers: chr11:g.72423820G>A (hg19) ; chr11:g.72712775G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712775G>A , CM000673.2:g.72712775G>A	GRCh38
NC_000011.9:g.72423820G>A , CM000673.1:g.72423820G>A	GRCh37
NC_000011.8:g.72101468G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393609.8:c.748-207C>T MANE Select	ENSP00000377233.3:n.748-207C>T
ENST00000334211.12:c.13-207C>T	ENSP00000335506.8:n.13-207C>T
ENST00000359373.9:c.748-207C>T	ENSP00000352332.5:n.748-207C>T
ENST00000393605.7:c.-180C>T	ENSP00000377230.3:n.-180C>T
ENST00000393609.7:c.748-207C>T	ENSP00000377233.3:n.748-207C>T
ENST00000426523.5:c.13-207C>T	ENSP00000392264.1:n.13-207C>T
ENST00000429686.5:c.13-207C>T	ENSP00000403127.1:n.13-207C>T
ENST00000465814.5:n.878C>T
NM_001040118.2:c.748-207C>T	NP_001035207.1:n.748-207C>T
NM_001135190.1:c.13-207C>T	NP_001128662.1:n.13-207C>T
NM_015242.4:c.13-207C>T	NP_056057.2:n.13-207C>T
NM_001369489.1:c.13-207C>T	NP_001356418.1:n.13-207C>T
NR_161388.1:n.730-207C>T
NM_001040118.3:c.748-207C>T MANE Select	NP_001035207.1:n.748-207C>T
NM_001135190.2:c.13-207C>T	NP_001128662.1:n.13-207C>T
NM_015242.5:c.13-207C>T	NP_056057.2:n.13-207C>T