Canonical Allele Identifier: CA2566799112

Gene: PRR16

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.120601916del , CM000667.2:g.120601916del	GRCh38
NC_000005.9:g.119937611del , CM000667.1:g.119937611del	GRCh37
NC_000005.8:g.119965510del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000407149.7:c.160-84038del MANE Select	ENSP00000385118.2:n.160-84038del
ENST00000379551.2:c.91-84038del	ENSP00000368869.2:n.91-84038del
ENST00000407149.6:c.160-84038del	ENSP00000385118.2:n.160-84038del
ENST00000505123.5:c.-273-15179del	ENSP00000423446.1:n.-273-15179del
ENST00000509923.1:c.-51-84038del	ENSP00000421256.1:n.-51-84038del
NM_001300783.1:c.160-84038del	NP_001287712.1:n.160-84038del
NM_001308087.1:c.-51-84038del	NP_001295016.1:n.-51-84038del
NM_001308088.1:c.-273-15179del	NP_001295017.1:n.-273-15179del
NM_016644.2:c.91-84038del	NP_057728.1:n.91-84038del
XM_005272012.2:c.-273-15179del	XP_005272069.1:n.-273-15179del
XM_011543452.1:c.-86-15179del	XP_011541754.1:n.-86-15179del
XM_011543453.1:c.-86-15179del	XP_011541755.1:n.-86-15179del
XM_011543454.1:c.-273-15179del	XP_011541756.1:n.-273-15179del
XM_011543456.1:c.-610-15179del	XP_011541758.1:n.-610-15179del
XM_011543452.2:c.-86-15179del	XP_011541754.1:n.-86-15179del
XM_011543453.3:c.-86-15179del	XP_011541755.1:n.-86-15179del
XM_011543454.2:c.-273-15179del	XP_011541756.1:n.-273-15179del
XR_001742093.1:n.425-84038del
XR_001742094.1:n.82-84038del
NM_001300783.2:c.160-84038del MANE Select	NP_001287712.1:n.160-84038del