Canonical Allele Identifier: CA1981895237
Gene: INPPL1 HGNC NCBI

Linked Data

dbSNP Id: rs1472993868

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72224745C>G , CM000673.2:g.72224745C>G GRCh38
NC_000011.9:g.71935789C>G , CM000673.1:g.71935789C>G GRCh37
NC_000011.8:g.71613437C>G NCBI36
NG_023253.1:g.4908C>G
NG_023253.2:g.4908C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000540973.1:c.-205-35C>G ENSP00000440904.1:n.-205-35C>G
ENST00000543234.1:c.-205-35C>G ENSP00000440512.1:n.-205-35C>G
XM_005273978.3:c.-205-35C>G XP_005274035.1:n.-205-35C>G
XM_005273979.3:c.-205-35C>G XP_005274036.1:n.-205-35C>G
XM_011544999.1:c.-205-35C>G XP_011543301.1:n.-205-35C>G
XM_011545000.1:c.-205-35C>G XP_011543302.1:n.-205-35C>G
XM_005273979.4:c.-205-35C>G XP_005274036.1:n.-205-35C>G
XM_011544999.2:c.-205-35C>G XP_011543301.1:n.-205-35C>G
XM_024448501.1:c.-205-35C>G XP_024304269.1:n.-205-35C>G
XM_024448502.1:c.-205-35C>G XP_024304270.1:n.-205-35C>G
XM_024448503.1:c.-326-35C>G XP_024304271.1:n.-326-35C>G
XM_024448504.1:c.-205-35C>G XP_024304272.1:n.-205-35C>G
XM_024448505.1:c.-205-35C>G XP_024304273.1:n.-205-35C>G