Canonical Allele Identifier: CA2842510857

Gene: PRR16

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.120601914T>C , CM000667.2:g.120601914T>C	GRCh38
NC_000005.9:g.119937609T>C , CM000667.1:g.119937609T>C	GRCh37
NC_000005.8:g.119965508T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407149.7:c.160-84040T>C MANE Select	ENSP00000385118.2:n.160-84040T>C
ENST00000379551.2:c.91-84040T>C	ENSP00000368869.2:n.91-84040T>C
ENST00000407149.6:c.160-84040T>C	ENSP00000385118.2:n.160-84040T>C
ENST00000505123.5:c.-273-15181T>C	ENSP00000423446.1:n.-273-15181T>C
ENST00000509923.1:c.-51-84040T>C	ENSP00000421256.1:n.-51-84040T>C
NM_001300783.1:c.160-84040T>C	NP_001287712.1:n.160-84040T>C
NM_001308087.1:c.-51-84040T>C	NP_001295016.1:n.-51-84040T>C
NM_001308088.1:c.-273-15181T>C	NP_001295017.1:n.-273-15181T>C
NM_016644.2:c.91-84040T>C	NP_057728.1:n.91-84040T>C
XM_005272012.2:c.-273-15181T>C	XP_005272069.1:n.-273-15181T>C
XM_011543452.1:c.-86-15181T>C	XP_011541754.1:n.-86-15181T>C
XM_011543453.1:c.-86-15181T>C	XP_011541755.1:n.-86-15181T>C
XM_011543454.1:c.-273-15181T>C	XP_011541756.1:n.-273-15181T>C
XM_011543456.1:c.-610-15181T>C	XP_011541758.1:n.-610-15181T>C
XM_011543452.2:c.-86-15181T>C	XP_011541754.1:n.-86-15181T>C
XM_011543453.3:c.-86-15181T>C	XP_011541755.1:n.-86-15181T>C
XM_011543454.2:c.-273-15181T>C	XP_011541756.1:n.-273-15181T>C
XR_001742093.1:n.425-84040T>C
XR_001742094.1:n.82-84040T>C
NM_001300783.2:c.160-84040T>C MANE Select	NP_001287712.1:n.160-84040T>C