Canonical Allele Identifier: CA372488982

Gene: PUF60

Linked Data

• MyVariant Identifiers: chr8:g.143817597C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143817597C>A , CM000670.2:g.143817597C>A	GRCh38
NC_000008.9:g.144971755C>A	NCBI36
NG_030583.1:g.2783G>T
NG_033879.1:g.16790G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000524570.6:n.1701G>T
ENST00000526151.6:n.3058G>T
ENST00000526459.6:c.949G>T	ENSP00000432610.2:p.Ala317Ser
ENST00000527744.6:c.1000G>T	ENSP00000436131.2:p.Ala334Ser
ENST00000531951.6:c.874G>T	ENSP00000515500.1:p.Ala292Ser
ENST00000532127.6:c.*848G>T	ENSP00000515484.1:n.*848G>T
ENST00000533162.2:c.1114G>T	ENSP00000433403.2:p.Ala372Ser
ENST00000533362.2:c.1078G>T	ENSP00000515502.1:p.Ala360Ser
ENST00000703744.1:n.1714G>T
ENST00000703803.1:n.1268G>T
ENST00000703846.1:c.874G>T	ENSP00000515498.1:p.Ala292Ser
ENST00000703847.1:c.1114G>T	ENSP00000515499.1:p.Ala372Ser
ENST00000703848.1:n.1034G>T
ENST00000703849.1:c.874G>T	ENSP00000515501.1:p.Ala292Ser
ENST00000703850.1:c.1078G>T	ENSP00000515503.1:p.Ala360Ser
ENST00000703851.1:n.923G>T
ENST00000703866.1:c.1003G>T	ENSP00000515511.1:p.Ala335Ser
ENST00000526683.6:c.1003G>T MANE Select	ENSP00000434359.1:p.Ala335Ser
ENST00000313352.11:c.823G>T	ENSP00000322016.7:p.Ala275Ser
ENST00000349157.10:c.952G>T	ENSP00000322036.7:p.Ala318Ser
ENST00000453551.6:c.874G>T	ENSP00000402953.2:p.Ala292Ser
ENST00000456095.6:c.916G>T	ENSP00000395417.2:p.Ala306Ser
ENST00000524570.5:n.1689G>T
ENST00000526459.5:c.949G>T	ENSP00000432610.1:p.Ala317Ser
ENST00000526683.5:c.1003G>T	ENSP00000434359.1:p.Ala335Ser
ENST00000527197.5:c.865G>T	ENSP00000431960.1:p.Ala289Ser
ENST00000527744.5:c.996G>T
ENST00000532884.1:c.612G>T
NM_001136033.2:c.874G>T	NP_001129505.1:p.Ala292Ser
NM_001271096.1:c.949G>T	NP_001258025.1:p.Ala317Ser
NM_001271097.1:c.865G>T	NP_001258026.1:p.Ala289Ser
NM_001271098.1:c.1000G>T	NP_001258027.1:p.Ala334Ser
NM_001271099.1:c.916G>T	NP_001258028.1:p.Ala306Ser
NM_001271100.1:c.823G>T	NP_001258029.1:p.Ala275Ser
NM_014281.4:c.952G>T	NP_055096.2:p.Ala318Ser
NM_078480.2:c.1003G>T	NP_510965.1:p.Ala335Ser
XM_011516929.1:c.1114G>T	XP_011515231.1:p.Ala372Ser
XM_011516930.1:c.1063G>T	XP_011515232.1:p.Ala355Ser
NM_001362895.1:c.1114G>T	NP_001349824.1:p.Ala372Ser
NM_001362896.1:c.1114G>T	NP_001349825.1:p.Ala372Ser
NM_001362897.1:c.1063G>T	NP_001349826.1:p.Ala355Ser
XM_017013234.1:c.1114G>T	XP_016868723.1:p.Ala372Ser
XM_017013235.1:c.1078G>T	XP_016868724.1:p.Ala360Ser
XM_017013236.1:c.1063G>T	XP_016868725.1:p.Ala355Ser
XM_017013239.1:c.874G>T	XP_016868728.1:p.Ala292Ser
XM_017013240.1:c.823G>T	XP_016868729.1:p.Ala275Ser
NM_001136033.3:c.874G>T	NP_001129505.1:p.Ala292Ser
NM_001271096.2:c.949G>T	NP_001258025.1:p.Ala317Ser
NM_001271097.2:c.865G>T	NP_001258026.1:p.Ala289Ser
NM_001271098.2:c.1000G>T	NP_001258027.1:p.Ala334Ser
NM_001271099.2:c.916G>T	NP_001258028.1:p.Ala306Ser
NM_001271100.2:c.823G>T	NP_001258029.1:p.Ala275Ser
NM_001362895.2:c.1114G>T	NP_001349824.1:p.Ala372Ser
NM_001362896.2:c.1114G>T	NP_001349825.1:p.Ala372Ser
NM_001362897.2:c.1063G>T	NP_001349826.1:p.Ala355Ser
NM_014281.5:c.952G>T	NP_055096.2:p.Ala318Ser
NM_078480.3:c.1003G>T MANE Select	NP_510965.1:p.Ala335Ser