Canonical Allele Identifier: CA844102157

Gene: PPP1R9A

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95294544G>C , CM000669.2:g.95294544G>C	GRCh38
NC_000007.13:g.94923856G>C , CM000669.1:g.94923856G>C	GRCh37
NC_000007.12:g.94761792G>C	NCBI36
NG_015803.1:g.391908G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433360.6:c.*4241G>C MANE Select	ENSP00000405514.1:n.*4241G>C
ENST00000340694.8:c.*4241G>C	ENSP00000344524.4:n.*4241G>C
ENST00000433881.5:c.*4241G>C	ENSP00000398870.1:n.*4241G>C
ENST00000456331.6:c.*4241G>C	ENSP00000402893.2:n.*4241G>C
NM_001166160.1:c.*4241G>C	NP_001159632.1:n.*4241G>C
NM_001166161.1:c.*4241G>C	NP_001159633.1:n.*4241G>C
NM_001166162.1:c.*4241G>C	NP_001159634.1:n.*4241G>C
NM_001166163.1:c.*4241G>C	NP_001159635.1:n.*4241G>C
NM_017650.2:c.*4241G>C	NP_060120.2:n.*4241G>C
XM_011516380.1:c.*4241G>C	XP_011514682.1:n.*4241G>C
XM_011516381.1:c.*4241G>C	XP_011514683.1:n.*4241G>C
XM_011516382.1:c.*4241G>C	XP_011514684.1:n.*4241G>C
XM_011516383.1:c.*4241G>C	XP_011514685.1:n.*4241G>C
XM_011516384.1:c.*4241G>C	XP_011514686.1:n.*4241G>C
XM_011516385.1:c.*4241G>C	XP_011514687.1:n.*4241G>C
XM_011516386.1:c.*4241G>C	XP_011514688.1:n.*4241G>C
XM_011516387.1:c.*4241G>C	XP_011514689.1:n.*4241G>C
XM_011516388.1:c.*4241G>C	XP_011514690.1:n.*4241G>C
XM_011516389.1:c.*4241G>C	XP_011514691.1:n.*4241G>C
XM_011516390.1:c.*4241G>C	XP_011514692.1:n.*4241G>C
XM_011516391.1:c.*4241G>C	XP_011514693.1:n.*4241G>C
XM_011516392.1:c.*4241G>C	XP_011514694.1:n.*4241G>C
XM_011516393.1:c.*4241G>C	XP_011514695.1:n.*4241G>C
XM_011516394.1:c.*4241G>C	XP_011514696.1:n.*4241G>C
XM_011516382.2:c.*4241G>C	XP_011514684.1:n.*4241G>C
XM_017012394.1:c.*4241G>C	XP_016867883.1:n.*4241G>C
XM_017012395.1:c.*4241G>C	XP_016867884.1:n.*4241G>C
XM_017012397.1:c.*4241G>C	XP_016867886.1:n.*4241G>C
XM_017012398.1:c.*4241G>C	XP_016867887.1:n.*4241G>C
XM_017012399.1:c.*4241G>C	XP_016867888.1:n.*4241G>C
XM_017012400.1:c.*4241G>C	XP_016867889.1:n.*4241G>C
XM_017012401.1:c.*4241G>C	XP_016867890.1:n.*4241G>C
XM_017012403.1:c.*4241G>C	XP_016867892.1:n.*4241G>C
XM_017012404.1:c.*4241G>C	XP_016867893.1:n.*4241G>C
XM_017012405.1:c.*4241G>C	XP_016867894.1:n.*4241G>C
XM_017012406.1:c.*4241G>C	XP_016867895.1:n.*4241G>C
XM_017012407.1:c.*4241G>C	XP_016867896.1:n.*4241G>C
XM_017012408.1:c.*4241G>C	XP_016867897.1:n.*4241G>C
XM_017012410.2:c.*4241G>C	XP_016867899.1:n.*4241G>C
XM_017012411.2:c.*4241G>C	XP_016867900.1:n.*4241G>C
XM_024446825.1:c.*4241G>C	XP_024302593.1:n.*4241G>C
NM_001166160.2:c.*4241G>C MANE Select	NP_001159632.1:n.*4241G>C
NM_017650.3:c.*4241G>C	NP_060120.2:n.*4241G>C