Canonical Allele Identifier: CA1825987973

Gene: PUF60

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143817102_143817107delinsCGAGGG , CM000670.2:g.143817102_143817107delinsCGAGGG	GRCh38
NC_000008.9:g.144971260_144971265delinsCGAGGG	NCBI36
NG_030583.1:g.3273_3278delinsCCCTCG
NG_033879.1:g.17280_17285delinsCCCTCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000524570.6:n.1881_1886delinsCCCTCG
ENST00000526151.6:n.3238_3243delinsCCCTCG
ENST00000526459.6:c.1129_1134delinsCCCTCG	ENSP00000432610.2:p.Pro377=
ENST00000527744.6:c.1180_1185delinsCCCTCG	ENSP00000436131.2:p.Pro394=
ENST00000531951.6:c.1054_1059delinsCCCTCG	ENSP00000515500.1:p.Pro352=
ENST00000532127.6:c.*1028_*1033delinsCCCTCG	ENSP00000515484.1:n.*1028_*1033delinsCCCT...
ENST00000533162.2:c.1294_1299delinsCCCTCG	ENSP00000433403.2:p.Pro432=
ENST00000533362.2:c.1258_1263delinsCCCTCG	ENSP00000515502.1:p.Pro420=
ENST00000703744.1:n.1894_1899delinsCCCTCG
ENST00000703803.1:n.1448_1453delinsCCCTCG
ENST00000703846.1:c.1054_1059delinsCCCTCG	ENSP00000515498.1:p.Pro352=
ENST00000703847.1:c.1294_1299delinsCCCTCG	ENSP00000515499.1:p.Pro432=
ENST00000703848.1:n.1214_1219delinsCCCTCG
ENST00000703849.1:c.1054_1059delinsCCCTCG	ENSP00000515501.1:p.Pro352=
ENST00000703850.1:c.1258_1263delinsCCCTCG	ENSP00000515503.1:p.Pro420=
ENST00000703851.1:n.1103_1108delinsCCCTCG
ENST00000703866.1:c.1183_1188delinsCCCTCG	ENSP00000515511.1:p.Pro395=
ENST00000526683.6:c.1183_1188delinsCCCTCG MANE Select	ENSP00000434359.1:p.Pro395=
ENST00000313352.11:c.1003_1008delinsCCCTCG	ENSP00000322016.7:p.Pro335=
ENST00000349157.10:c.1132_1137delinsCCCTCG	ENSP00000322036.7:p.Pro378=
ENST00000453551.6:c.1054_1059delinsCCCTCG	ENSP00000402953.2:p.Pro352=
ENST00000456095.6:c.1096_1101delinsCCCTCG	ENSP00000395417.2:p.Pro366=
ENST00000524570.5:n.1869_1874delinsCCCTCG
ENST00000526683.5:c.1183_1188delinsCCCTCG	ENSP00000434359.1:p.Pro395=
ENST00000527197.5:c.1045_1050delinsCCCTCG	ENSP00000431960.1:p.Pro349=
ENST00000532884.1:c.792_797delinsCCCTCG
NM_001136033.2:c.1054_1059delinsCCCTCG	NP_001129505.1:p.Pro352=
NM_001271096.1:c.1129_1134delinsCCCTCG	NP_001258025.1:p.Pro377=
NM_001271097.1:c.1045_1050delinsCCCTCG	NP_001258026.1:p.Pro349=
NM_001271098.1:c.1180_1185delinsCCCTCG	NP_001258027.1:p.Pro394=
NM_001271099.1:c.1096_1101delinsCCCTCG	NP_001258028.1:p.Pro366=
NM_001271100.1:c.1003_1008delinsCCCTCG	NP_001258029.1:p.Pro335=
NM_014281.4:c.1132_1137delinsCCCTCG	NP_055096.2:p.Pro378=
NM_078480.2:c.1183_1188delinsCCCTCG	NP_510965.1:p.Pro395=
XM_011516929.1:c.1294_1299delinsCCCTCG	XP_011515231.1:p.Pro432=
XM_011516930.1:c.1243_1248delinsCCCTCG	XP_011515232.1:p.Pro415=
NM_001362895.1:c.1294_1299delinsCCCTCG	NP_001349824.1:p.Pro432=
NM_001362896.1:c.1294_1299delinsCCCTCG	NP_001349825.1:p.Pro432=
NM_001362897.1:c.1243_1248delinsCCCTCG	NP_001349826.1:p.Pro415=
XM_017013234.1:c.1294_1299delinsCCCTCG	XP_016868723.1:p.Pro432=
XM_017013235.1:c.1258_1263delinsCCCTCG	XP_016868724.1:p.Pro420=
XM_017013236.1:c.1243_1248delinsCCCTCG	XP_016868725.1:p.Pro415=
XM_017013239.1:c.1054_1059delinsCCCTCG	XP_016868728.1:p.Pro352=
XM_017013240.1:c.1003_1008delinsCCCTCG	XP_016868729.1:p.Pro335=
NM_001136033.3:c.1054_1059delinsCCCTCG	NP_001129505.1:p.Pro352=
NM_001271096.2:c.1129_1134delinsCCCTCG	NP_001258025.1:p.Pro377=
NM_001271097.2:c.1045_1050delinsCCCTCG	NP_001258026.1:p.Pro349=
NM_001271098.2:c.1180_1185delinsCCCTCG	NP_001258027.1:p.Pro394=
NM_001271099.2:c.1096_1101delinsCCCTCG	NP_001258028.1:p.Pro366=
NM_001271100.2:c.1003_1008delinsCCCTCG	NP_001258029.1:p.Pro335=
NM_001362895.2:c.1294_1299delinsCCCTCG	NP_001349824.1:p.Pro432=
NM_001362896.2:c.1294_1299delinsCCCTCG	NP_001349825.1:p.Pro432=
NM_001362897.2:c.1243_1248delinsCCCTCG	NP_001349826.1:p.Pro415=
NM_014281.5:c.1132_1137delinsCCCTCG	NP_055096.2:p.Pro378=
NM_078480.3:c.1183_1188delinsCCCTCG MANE Select	NP_510965.1:p.Pro395=