Canonical Allele Identifier: CA2792650521
Gene: INPPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72225147dup , CM000673.2:g.72225147dup GRCh38
NC_000011.9:g.71936191dup , CM000673.1:g.71936191dup GRCh37
NC_000011.8:g.71613839dup NCBI36
NG_023253.1:g.5310dup
NG_023253.2:g.5310dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000298229.7:c.163dup MANE Select ENSP00000298229.2:p.Ala55GlyfsTer20
ENST00000298229.6:c.163dup ENSP00000298229.2:p.Ala55GlyfsTer20
ENST00000541544.1:n.79dup
NM_001567.3:c.163dup NP_001558.3:p.Ala55GlyfsTer20
XM_005273978.3:c.163dup XP_005274035.1:p.Ala55GlyfsTer20
XM_005273979.3:c.163dup XP_005274036.1:p.Ala55GlyfsTer20
XM_011544999.1:c.163dup XP_011543301.1:p.Ala55GlyfsTer20
XM_011545000.1:c.163dup XP_011543302.1:p.Ala55GlyfsTer20
XM_005273979.4:c.163dup XP_005274036.1:p.Ala55GlyfsTer20
XM_011544999.2:c.163dup XP_011543301.1:p.Ala55GlyfsTer20
XM_024448501.1:c.163dup XP_024304269.1:p.Ala55GlyfsTer20
XM_024448502.1:c.163dup XP_024304270.1:p.Ala55GlyfsTer20
XM_024448503.1:c.42dup XP_024304271.1:p.Pro15AlafsTer15
XM_024448504.1:c.163dup XP_024304272.1:p.Ala55GlyfsTer20
XM_024448505.1:c.163dup XP_024304273.1:p.Ala55GlyfsTer20
NM_001567.4:c.163dup MANE Select NP_001558.3:p.Ala55GlyfsTer20