Canonical Allele Identifier: CA6699307

Gene: PPP1R12A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.79779349C>T , CM000674.2:g.79779349C>T	GRCh38
NC_000012.11:g.80173129C>T , CM000674.1:g.80173129C>T	GRCh37
NC_000012.10:g.78697260C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002480.3:c.2956-749G>A MANE Select	NP_002471.1:n.2956-749G>A
ENST00000450142.7:c.2956-749G>A MANE Select	ENSP00000389168.2:n.2956-749G>A
NM_001143885.1:c.2956-749G>A	NP_001137357.1:n.2956-749G>A
NM_001143885.2:c.2956-749G>A	NP_001137357.1:n.2956-749G>A
NM_001143886.1:c.2695-749G>A	NP_001137358.1:n.2695-749G>A
NM_001143886.2:c.2695-749G>A	NP_001137358.1:n.2695-749G>A
NM_001244990.1:c.2851-749G>A	NP_001231919.1:n.2851-749G>A
NM_001244990.2:c.2851-749G>A	NP_001231919.1:n.2851-749G>A
NM_001244992.1:c.2788-749G>A	NP_001231921.1:n.2788-749G>A
NM_002480.2:c.2956-749G>A	NP_002471.1:n.2956-749G>A
ENST00000261207.9:c.2956-749G>A	ENSP00000261207.5:n.2956-749G>A
ENST00000437004.6:c.2851-749G>A	ENSP00000416769.2:n.2851-749G>A
ENST00000450142.6:c.2956-749G>A	ENSP00000389168.2:n.2956-749G>A
ENST00000546369.5:c.2695-749G>A	ENSP00000449514.1:n.2695-749G>A
ENST00000546762.5:c.732-749G>A
ENST00000547253.5:n.528-749G>A
ENST00000548908.2:n.2182G>A
ENST00000548908.3:n.2180G>A
ENST00000550107.5:c.2788-749G>A	ENSP00000446855.1:n.2788-749G>A
ENST00000550299.5:c.506G>A
ENST00000550351.5:n.590-749G>A
ENST00000550903.5:c.807-749G>A	ENSP00000449647.1:n.807-749G>A
ENST00000552892.1:n.1397G>A
ENST00000634739.1:c.261G>A	ENSP00000489242.1:p.Val87=
XM_005268887.2:c.2958G>A	XP_005268944.1:p.Val986=
XM_005268887.4:c.2958G>A	XP_005268944.1:p.Val986=
XM_011538374.1:c.3073-749G>A	XP_011536676.1:n.3073-749G>A
XM_011538374.2:c.3073-749G>A	XP_011536676.1:n.3073-749G>A
XM_011538375.1:c.3037-749G>A	XP_011536677.1:n.3037-749G>A
XM_011538375.2:c.3037-749G>A	XP_011536677.1:n.3037-749G>A
XM_011538376.1:c.3075G>A	XP_011536678.1:p.Val1025=
XM_011538376.3:c.3075G>A	XP_011536678.1:p.Val1025=
XM_011538377.1:c.2998-749G>A	XP_011536679.1:n.2998-749G>A
XM_011538377.2:c.2998-749G>A	XP_011536679.1:n.2998-749G>A
XM_011538378.1:c.3075G>A	XP_011536680.1:p.Val1025=
XM_011538378.3:c.3075G>A	XP_011536680.1:p.Val1025=
XM_011538379.1:c.2905-749G>A	XP_011536681.1:n.2905-749G>A
XM_011538379.2:c.2905-749G>A	XP_011536681.1:n.2905-749G>A
XM_011538380.1:c.2896-749G>A	XP_011536682.1:n.2896-749G>A
XM_011538380.2:c.2896-749G>A	XP_011536682.1:n.2896-749G>A
XM_011538381.1:c.2812-749G>A	XP_011536683.1:n.2812-749G>A
XM_011538383.1:c.2779-749G>A	XP_011536685.1:n.2779-749G>A
XM_011538383.3:c.2779-749G>A	XP_011536685.1:n.2779-749G>A
XM_011538384.1:c.2728-749G>A	XP_011536686.1:n.2728-749G>A
XM_011538384.2:c.2728-749G>A	XP_011536686.1:n.2728-749G>A
XM_011538385.1:c.2611-749G>A	XP_011536687.1:n.2611-749G>A
XM_011538385.2:c.2611-749G>A	XP_011536687.1:n.2611-749G>A
XM_017019323.2:c.2920-749G>A	XP_016874812.1:n.2920-749G>A
XM_017019324.2:c.2881-749G>A	XP_016874813.1:n.2881-749G>A
XM_017019325.2:c.2845-749G>A	XP_016874814.1:n.2845-749G>A
XM_017019326.2:c.2743-749G>A	XP_016874815.1:n.2743-749G>A
XM_017019327.2:c.2790G>A	XP_016874816.1:p.Val930=
XM_017019328.2:c.2713-749G>A	XP_016874817.1:n.2713-749G>A
XM_017019329.2:c.2704-749G>A	XP_016874818.1:n.2704-749G>A
XR_001748712.2:n.4947G>A
XR_944554.1:n.3412-749G>A