Canonical Allele Identifier: CA381734277

Gene: INPPL1

Linked Data

• dbSNP Id: rs368970014
• gnomAD v4: 11-72234531-C-G
• MyVariant Identifiers: chr11:g.71945575C>G (hg19) ; chr11:g.72234531C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72234531C>G , CM000673.2:g.72234531C>G	GRCh38
NC_000011.9:g.71945575C>G , CM000673.1:g.71945575C>G	GRCh37
NC_000011.8:g.71623223C>G	NCBI36
NG_023253.1:g.14694C>G
NG_023253.2:g.14694C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.2331C>G MANE Select	ENSP00000298229.2:p.Tyr777Ter
ENST00000298229.6:c.2331C>G	ENSP00000298229.2:p.Tyr777Ter
ENST00000535985.1:c.184C>G
ENST00000538751.5:c.1605C>G	ENSP00000444619.1:p.Tyr535Ter
ENST00000541303.5:n.937C>G
ENST00000541756.5:c.2133C>G	ENSP00000446360.2:p.Tyr711Ter
ENST00000545355.5:n.616C>G
NM_001567.3:c.2331C>G	NP_001558.3:p.Tyr777Ter
XM_005273978.3:c.2397C>G	XP_005274035.1:p.Tyr799Ter
XM_005273979.3:c.2397C>G	XP_005274036.1:p.Tyr799Ter
XM_011544999.1:c.2331C>G	XP_011543301.1:p.Tyr777Ter
XM_011545000.1:c.2397C>G	XP_011543302.1:p.Tyr799Ter
XM_005273979.4:c.2397C>G	XP_005274036.1:p.Tyr799Ter
XM_011544999.2:c.2331C>G	XP_011543301.1:p.Tyr777Ter
XM_024448501.1:c.2529C>G	XP_024304269.1:p.Tyr843Ter
XM_024448502.1:c.2529C>G	XP_024304270.1:p.Tyr843Ter
XM_024448503.1:c.2499C>G	XP_024304271.1:p.Tyr833Ter
XM_024448504.1:c.2463C>G	XP_024304272.1:p.Tyr821Ter
XM_024448505.1:c.2529C>G	XP_024304273.1:p.Tyr843Ter
NM_001567.4:c.2331C>G MANE Select	NP_001558.3:p.Tyr777Ter