Canonical Allele Identifier: CA475606350

Gene: INPPL1

Linked Data

• MyVariant Identifiers: chr11:g.71936199G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225155G>C , CM000673.2:g.72225155G>C	GRCh38
NC_000011.9:g.71936199G>C , CM000673.1:g.71936199G>C	GRCh37
NC_000011.8:g.71613847G>C	NCBI36
NG_023253.1:g.5318G>C
NG_023253.2:g.5318G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.171G>C MANE Select	ENSP00000298229.2:p.Ala57=
ENST00000298229.6:c.171G>C	ENSP00000298229.2:p.Ala57=
ENST00000541544.1:n.87G>C
NM_001567.3:c.171G>C	NP_001558.3:p.Ala57=
XM_005273978.3:c.171G>C	XP_005274035.1:p.Ala57=
XM_005273979.3:c.171G>C	XP_005274036.1:p.Ala57=
XM_011544999.1:c.171G>C	XP_011543301.1:p.Ala57=
XM_011545000.1:c.171G>C	XP_011543302.1:p.Ala57=
XM_005273979.4:c.171G>C	XP_005274036.1:p.Ala57=
XM_011544999.2:c.171G>C	XP_011543301.1:p.Ala57=
XM_024448501.1:c.171G>C	XP_024304269.1:p.Ala57=
XM_024448502.1:c.171G>C	XP_024304270.1:p.Ala57=
XM_024448503.1:c.50G>C	XP_024304271.1:p.Arg17Pro
XM_024448504.1:c.171G>C	XP_024304272.1:p.Ala57=
XM_024448505.1:c.171G>C	XP_024304273.1:p.Ala57=
NM_001567.4:c.171G>C MANE Select	NP_001558.3:p.Ala57=