Canonical Allele Identifier: CA2579986031

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961036_87961037delinsGG , CM000672.2:g.87961036_87961037delinsGG	GRCh38
NC_000010.10:g.89720793_89720794delinsGG , CM000672.1:g.89720793_89720794delinsGG	GRCh37
NC_000010.9:g.89710773_89710774delinsGG	NCBI36
NG_007466.2:g.102598_102599delinsGG , LRG_311:g.102598_102599delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1037_1038delinsGG	ENSP00000514759.2:p.Tyr346Trp
ENST00000710265.1:c.944_945delinsGG	ENSP00000518161.1:p.Tyr315Trp
ENST00000472832.3:c.944_945delinsGG	ENSP00000483066.2:p.Tyr315Trp
ENST00000688158.2:n.1679_1680delinsGG
ENST00000688922.2:c.*774_*775delinsGG	ENSP00000508742.2:n.*774_*775delinsGG
ENST00000700021.1:c.899_900delinsGG	ENSP00000514757.1:p.Tyr300Trp
ENST00000700022.1:c.*283_*284delinsGG	ENSP00000514758.1:n.*283_*284delinsGG
ENST00000700023.1:n.2102_2103delinsGG
ENST00000700024.1:n.2336_2337delinsGG
ENST00000700025.1:n.1713_1714delinsGG
ENST00000700026.1:n.581_582delinsGG
ENST00000706954.1:c.944_945delinsGG	ENSP00000516674.1:p.Tyr315Trp
ENST00000706955.1:c.*979_*980delinsGG	ENSP00000516675.1:n.*979_*980delinsGG
ENST00000686459.1:c.*530_*531delinsGG	ENSP00000508909.1:n.*530_*531delinsGG
ENST00000688158.1:c.*1055_*1056delinsGG	ENSP00000509254.1:n.*1055_*1056delinsGG
ENST00000688308.1:c.944_945delinsGG	ENSP00000508752.1:p.Tyr315Trp
ENST00000688922.1:c.865_866delinsGG
ENST00000693560.1:c.1463_1464delinsGG	ENSP00000509861.1:p.Tyr488Trp
ENST00000371953.8:c.944_945delinsGG MANE Select	ENSP00000361021.3:p.Tyr315Trp
ENST00000371953.7:c.944_945delinsGG	ENSP00000361021.3:p.Tyr315Trp
ENST00000472832.2:c.371_372delinsGG	ENSP00000483066.1:p.Tyr124Trp
NM_000314.5:c.944_945delinsGG	NP_000305.3:p.Tyr315Trp
NM_000314.6:c.944_945delinsGG	NP_000305.3:p.Tyr315Trp
NM_001304717.2:c.1463_1464delinsGG	NP_001291646.2:p.Tyr488Trp
NM_001304718.1:c.353_354delinsGG	NP_001291647.1:p.Tyr118Trp
XM_006717926.2:c.899_900delinsGG	XP_006717989.1:p.Tyr300Trp
XM_011539981.1:c.944_945delinsGG	XP_011538283.1:p.Tyr315Trp
XM_011539982.1:c.848_849delinsGG	XP_011538284.1:p.Tyr283Trp
XR_945791.1:n.1514_1515delinsGG
NM_000314.7:c.944_945delinsGG	NP_000305.3:p.Tyr315Trp
NM_001304717.5:c.1463_1464delinsGG	NP_001291646.4:p.Tyr488Trp
NM_001304718.2:c.353_354delinsGG	NP_001291647.1:p.Tyr118Trp
NM_000314.8:c.944_945delinsGG MANE Select	NP_000305.3:p.Tyr315Trp