Canonical Allele Identifier: CA3382939

Gene: PRR16

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.120686030C>T , CM000667.2:g.120686030C>T	GRCh38
NC_000005.9:g.120021725C>T , CM000667.1:g.120021725C>T	GRCh37
NC_000005.8:g.120049624C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001300783.2:c.236C>T MANE Select	NP_001287712.1:p.Thr79Met
ENST00000407149.7:c.236C>T MANE Select	ENSP00000385118.2:p.Thr79Met
NM_001300783.1:c.236C>T	NP_001287712.1:p.Thr79Met
NM_001308087.1:c.26C>T	NP_001295016.1:p.Thr9Met
NM_001308088.1:c.26C>T	NP_001295017.1:p.Thr9Met
NM_016644.2:c.167C>T	NP_057728.1:p.Thr56Met
ENST00000379551.2:c.167C>T	ENSP00000368869.2:p.Thr56Met
ENST00000407149.6:c.236C>T	ENSP00000385118.2:p.Thr79Met
ENST00000446965.2:c.77C>T	ENSP00000405491.2:p.Thr26Met
ENST00000505123.5:c.26C>T	ENSP00000423446.1:p.Thr9Met
ENST00000509923.1:c.26C>T	ENSP00000421256.1:p.Thr9Met
XM_005272012.2:c.26C>T	XP_005272069.1:p.Thr9Met
XM_011543452.1:c.89C>T	XP_011541754.1:p.Thr30Met
XM_011543452.2:c.89C>T	XP_011541754.1:p.Thr30Met
XM_011543453.1:c.89C>T	XP_011541755.1:p.Thr30Met
XM_011543453.3:c.89C>T	XP_011541755.1:p.Thr30Met
XM_011543454.1:c.26C>T	XP_011541756.1:p.Thr9Met
XM_011543454.2:c.26C>T	XP_011541756.1:p.Thr9Met
XM_011543455.1:c.26C>T	XP_011541757.1:p.Thr9Met
XM_011543456.1:c.26C>T	XP_011541758.1:p.Thr9Met
XR_001742093.1:n.501C>T
XR_001742094.1:n.158C>T