Canonical Allele Identifier: CA2541265034

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460672_80460673insTTCTCATA , CM000674.2:g.80460672_80460673insTTCTCATA	GRCh38
NC_000012.11:g.80849504_80849505insTATGAGAA , CM000674.1:g.80849504_80849505insTATGAGAA	GRCh37
NC_000012.10:g.79373635_79373636insTATGAGAA	NCBI36
NG_034052.1:g.21327_21328insTTCTCATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.680_681insTTCTCATA MANE Select	ENSP00000495607.1:p.Leu227PhefsTer30
ENST00000614701.4:c.680_681insTTCTCATA	ENSP00000482885.1:p.Leu227PhefsTer30
ENST00000616559.4:c.806_807insTTCTCATA	ENSP00000483259.1:p.Leu269PhefsTer30
NM_001145026.1:c.680_681insTTCTCATA	NP_001138498.1:p.Leu227PhefsTer30
XM_011538290.1:c.680_681insTTCTCATA	XP_011536592.1:p.Leu227PhefsTer30
XM_017019273.1:c.1346_1347insTTCTCATA	XP_016874762.1:p.Leu449PhefsTer30
XM_017019274.1:c.1346_1347insTTCTCATA	XP_016874763.1:p.Leu449PhefsTer30
XM_017019275.1:c.1346_1347insTTCTCATA	XP_016874764.1:p.Leu449PhefsTer30
XR_001748688.1:n.1483_1484insTTCTCATA
XR_001748689.1:n.1483_1484insTTCTCATA
NM_001145026.2:c.680_681insTTCTCATA MANE Select	NP_001138498.1:p.Leu227PhefsTer30