Canonical Allele Identifier: CA372492474

Gene: PUF60

Linked Data

• MyVariant Identifiers: chr8:g.143818214C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143818214C>T , CM000670.2:g.143818214C>T	GRCh38
NC_000008.9:g.144972372C>T	NCBI36
NG_030583.1:g.2166G>A
NG_033879.1:g.16173G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000524570.6:n.1280G>A
ENST00000526151.6:n.2637G>A
ENST00000526459.6:c.528G>A	ENSP00000432610.2:p.Met176Ile
ENST00000527744.6:c.579G>A	ENSP00000436131.2:p.Met193Ile
ENST00000531951.6:c.453G>A	ENSP00000515500.1:p.Met151Ile
ENST00000532127.6:c.*427G>A	ENSP00000515484.1:n.*427G>A
ENST00000533162.2:c.693G>A	ENSP00000433403.2:p.Met231Ile
ENST00000533362.2:c.657G>A	ENSP00000515502.1:p.Met219Ile
ENST00000703744.1:n.1293G>A
ENST00000703803.1:n.730G>A
ENST00000703846.1:c.453G>A	ENSP00000515498.1:p.Met151Ile
ENST00000703847.1:c.693G>A	ENSP00000515499.1:p.Met231Ile
ENST00000703848.1:n.613G>A
ENST00000703849.1:c.453G>A	ENSP00000515501.1:p.Met151Ile
ENST00000703850.1:c.657G>A	ENSP00000515503.1:p.Met219Ile
ENST00000703851.1:n.502G>A
ENST00000703852.1:c.*505G>A	ENSP00000515504.1:n.*505G>A
ENST00000703853.1:n.496G>A
ENST00000703866.1:c.582G>A	ENSP00000515511.1:p.Met194Ile
ENST00000526683.6:c.582G>A MANE Select	ENSP00000434359.1:p.Met194Ile
ENST00000313352.11:c.402G>A	ENSP00000322016.7:p.Met134Ile
ENST00000349157.10:c.531G>A	ENSP00000322036.7:p.Met177Ile
ENST00000453551.6:c.453G>A	ENSP00000402953.2:p.Met151Ile
ENST00000456095.6:c.495G>A	ENSP00000395417.2:p.Met165Ile
ENST00000524570.5:n.1268G>A
ENST00000526459.5:c.528G>A	ENSP00000432610.1:p.Met176Ile
ENST00000526683.5:c.582G>A	ENSP00000434359.1:p.Met194Ile
ENST00000527197.5:c.444G>A	ENSP00000431960.1:p.Met148Ile
ENST00000527744.5:c.575G>A
ENST00000528320.5:n.594G>A
ENST00000528999.5:n.313G>A
ENST00000529693.1:n.663G>A
ENST00000529999.5:c.642G>A	ENSP00000434863.1:p.Met214Ile
ENST00000531897.5:c.642G>A	ENSP00000437309.1:p.Met214Ile
ENST00000531951.5:n.742G>A
ENST00000532884.1:c.176G>A
NM_001136033.2:c.453G>A	NP_001129505.1:p.Met151Ile
NM_001271096.1:c.528G>A	NP_001258025.1:p.Met176Ile
NM_001271097.1:c.444G>A	NP_001258026.1:p.Met148Ile
NM_001271098.1:c.579G>A	NP_001258027.1:p.Met193Ile
NM_001271099.1:c.495G>A	NP_001258028.1:p.Met165Ile
NM_001271100.1:c.402G>A	NP_001258029.1:p.Met134Ile
NM_014281.4:c.531G>A	NP_055096.2:p.Met177Ile
NM_078480.2:c.582G>A	NP_510965.1:p.Met194Ile
XM_011516929.1:c.693G>A	XP_011515231.1:p.Met231Ile
XM_011516930.1:c.642G>A	XP_011515232.1:p.Met214Ile
NM_001362895.1:c.693G>A	NP_001349824.1:p.Met231Ile
NM_001362896.1:c.693G>A	NP_001349825.1:p.Met231Ile
NM_001362897.1:c.642G>A	NP_001349826.1:p.Met214Ile
XM_017013234.1:c.693G>A	XP_016868723.1:p.Met231Ile
XM_017013235.1:c.657G>A	XP_016868724.1:p.Met219Ile
XM_017013236.1:c.642G>A	XP_016868725.1:p.Met214Ile
XM_017013239.1:c.453G>A	XP_016868728.1:p.Met151Ile
XM_017013240.1:c.402G>A	XP_016868729.1:p.Met134Ile
NM_001136033.3:c.453G>A	NP_001129505.1:p.Met151Ile
NM_001271096.2:c.528G>A	NP_001258025.1:p.Met176Ile
NM_001271097.2:c.444G>A	NP_001258026.1:p.Met148Ile
NM_001271098.2:c.579G>A	NP_001258027.1:p.Met193Ile
NM_001271099.2:c.495G>A	NP_001258028.1:p.Met165Ile
NM_001271100.2:c.402G>A	NP_001258029.1:p.Met134Ile
NM_001362895.2:c.693G>A	NP_001349824.1:p.Met231Ile
NM_001362896.2:c.693G>A	NP_001349825.1:p.Met231Ile
NM_001362897.2:c.642G>A	NP_001349826.1:p.Met214Ile
NM_014281.5:c.531G>A	NP_055096.2:p.Met177Ile
NM_078480.3:c.582G>A MANE Select	NP_510965.1:p.Met194Ile