Canonical Allele Identifier: CA381722815

Gene: INPPL1

Linked Data

• MyVariant Identifiers: chr11:g.71940989A>C (hg19) ; chr11:g.72229945A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229945A>C , CM000673.2:g.72229945A>C	GRCh38
NC_000011.9:g.71940989A>C , CM000673.1:g.71940989A>C	GRCh37
NC_000011.8:g.71618637A>C	NCBI36
NG_023253.1:g.10108A>C
NG_023253.2:g.10108A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.865A>C MANE Select	ENSP00000298229.2:p.Met289Leu
ENST00000298229.6:c.865A>C	ENSP00000298229.2:p.Met289Leu
ENST00000538751.5:c.139A>C	ENSP00000444619.1:p.Met47Leu
ENST00000540329.5:c.49A>C	ENSP00000440018.1:p.Met17Leu
ENST00000541756.5:c.667A>C	ENSP00000446360.2:p.Met223Leu
NM_001567.3:c.865A>C	NP_001558.3:p.Met289Leu
XM_005273978.3:c.931A>C	XP_005274035.1:p.Met311Leu
XM_005273979.3:c.931A>C	XP_005274036.1:p.Met311Leu
XM_011544999.1:c.865A>C	XP_011543301.1:p.Met289Leu
XM_011545000.1:c.931A>C	XP_011543302.1:p.Met311Leu
XM_005273979.4:c.931A>C	XP_005274036.1:p.Met311Leu
XM_011544999.2:c.865A>C	XP_011543301.1:p.Met289Leu
XM_024448501.1:c.931A>C	XP_024304269.1:p.Met311Leu
XM_024448502.1:c.931A>C	XP_024304270.1:p.Met311Leu
XM_024448503.1:c.901A>C	XP_024304271.1:p.Met301Leu
XM_024448504.1:c.865A>C	XP_024304272.1:p.Met289Leu
XM_024448505.1:c.931A>C	XP_024304273.1:p.Met311Leu
NM_001567.4:c.865A>C MANE Select	NP_001558.3:p.Met289Leu