Canonical Allele Identifier: CA372492519

Gene: PUF60

Linked Data

• MyVariant Identifiers: chr8:g.143818224T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143818224T>G , CM000670.2:g.143818224T>G	GRCh38
NC_000008.9:g.144972382T>G	NCBI36
NG_030583.1:g.2156A>C
NG_033879.1:g.16163A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000524570.6:n.1270A>C
ENST00000526151.6:n.2627A>C
ENST00000526459.6:c.518A>C	ENSP00000432610.2:p.Asn173Thr
ENST00000527744.6:c.569A>C	ENSP00000436131.2:p.Asn190Thr
ENST00000531951.6:c.443A>C	ENSP00000515500.1:p.Asn148Thr
ENST00000532127.6:c.*417A>C	ENSP00000515484.1:n.*417A>C
ENST00000533162.2:c.683A>C	ENSP00000433403.2:p.Asn228Thr
ENST00000533362.2:c.647A>C	ENSP00000515502.1:p.Asn216Thr
ENST00000703744.1:n.1283A>C
ENST00000703803.1:n.720A>C
ENST00000703846.1:c.443A>C	ENSP00000515498.1:p.Asn148Thr
ENST00000703847.1:c.683A>C	ENSP00000515499.1:p.Asn228Thr
ENST00000703848.1:n.603A>C
ENST00000703849.1:c.443A>C	ENSP00000515501.1:p.Asn148Thr
ENST00000703850.1:c.647A>C	ENSP00000515503.1:p.Asn216Thr
ENST00000703851.1:n.492A>C
ENST00000703852.1:c.*495A>C	ENSP00000515504.1:n.*495A>C
ENST00000703853.1:n.486A>C
ENST00000703866.1:c.572A>C	ENSP00000515511.1:p.Asn191Thr
ENST00000526683.6:c.572A>C MANE Select	ENSP00000434359.1:p.Asn191Thr
ENST00000313352.11:c.392A>C	ENSP00000322016.7:p.Asn131Thr
ENST00000349157.10:c.521A>C	ENSP00000322036.7:p.Asn174Thr
ENST00000453551.6:c.443A>C	ENSP00000402953.2:p.Asn148Thr
ENST00000456095.6:c.485A>C	ENSP00000395417.2:p.Asn162Thr
ENST00000524570.5:n.1258A>C
ENST00000526459.5:c.518A>C	ENSP00000432610.1:p.Asn173Thr
ENST00000526683.5:c.572A>C	ENSP00000434359.1:p.Asn191Thr
ENST00000527197.5:c.434A>C	ENSP00000431960.1:p.Asn145Thr
ENST00000527744.5:c.565A>C
ENST00000528320.5:n.584A>C
ENST00000528999.5:n.303A>C
ENST00000529693.1:n.653A>C
ENST00000529999.5:c.632A>C	ENSP00000434863.1:p.Asn211Thr
ENST00000531897.5:c.632A>C	ENSP00000437309.1:p.Asn211Thr
ENST00000531951.5:n.732A>C
ENST00000532884.1:c.166A>C
ENST00000533162.1:c.683A>C	ENSP00000433403.1:p.Asn228Thr
NM_001136033.2:c.443A>C	NP_001129505.1:p.Asn148Thr
NM_001271096.1:c.518A>C	NP_001258025.1:p.Asn173Thr
NM_001271097.1:c.434A>C	NP_001258026.1:p.Asn145Thr
NM_001271098.1:c.569A>C	NP_001258027.1:p.Asn190Thr
NM_001271099.1:c.485A>C	NP_001258028.1:p.Asn162Thr
NM_001271100.1:c.392A>C	NP_001258029.1:p.Asn131Thr
NM_014281.4:c.521A>C	NP_055096.2:p.Asn174Thr
NM_078480.2:c.572A>C	NP_510965.1:p.Asn191Thr
XM_011516929.1:c.683A>C	XP_011515231.1:p.Asn228Thr
XM_011516930.1:c.632A>C	XP_011515232.1:p.Asn211Thr
NM_001362895.1:c.683A>C	NP_001349824.1:p.Asn228Thr
NM_001362896.1:c.683A>C	NP_001349825.1:p.Asn228Thr
NM_001362897.1:c.632A>C	NP_001349826.1:p.Asn211Thr
XM_017013234.1:c.683A>C	XP_016868723.1:p.Asn228Thr
XM_017013235.1:c.647A>C	XP_016868724.1:p.Asn216Thr
XM_017013236.1:c.632A>C	XP_016868725.1:p.Asn211Thr
XM_017013239.1:c.443A>C	XP_016868728.1:p.Asn148Thr
XM_017013240.1:c.392A>C	XP_016868729.1:p.Asn131Thr
NM_001136033.3:c.443A>C	NP_001129505.1:p.Asn148Thr
NM_001271096.2:c.518A>C	NP_001258025.1:p.Asn173Thr
NM_001271097.2:c.434A>C	NP_001258026.1:p.Asn145Thr
NM_001271098.2:c.569A>C	NP_001258027.1:p.Asn190Thr
NM_001271099.2:c.485A>C	NP_001258028.1:p.Asn162Thr
NM_001271100.2:c.392A>C	NP_001258029.1:p.Asn131Thr
NM_001362895.2:c.683A>C	NP_001349824.1:p.Asn228Thr
NM_001362896.2:c.683A>C	NP_001349825.1:p.Asn228Thr
NM_001362897.2:c.632A>C	NP_001349826.1:p.Asn211Thr
NM_014281.5:c.521A>C	NP_055096.2:p.Asn174Thr
NM_078480.3:c.572A>C MANE Select	NP_510965.1:p.Asn191Thr