Canonical Allele Identifier: CA15388136

Gene: CSNK1G3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.123519722G>A , CM000667.2:g.123519722G>A	GRCh38
NC_000005.9:g.122855416G>A , CM000667.1:g.122855416G>A	GRCh37
NC_000005.8:g.122883315G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345990.9:c.-248+7152G>A	ENSP00000334735.5:n.-248+7152G>A
ENST00000696905.1:c.-248+7152G>A MANE Select	ENSP00000512966.1:n.-248+7152G>A
ENST00000345990.8:c.-248+7152G>A	ENSP00000334735.4:n.-248+7152G>A
ENST00000508708.1:n.380+7152G>A
ENST00000511130.6:c.-51+7152G>A	ENSP00000421385.2:n.-51+7152G>A
ENST00000512718.7:c.-48+7152G>A	ENSP00000421998.3:n.-48+7152G>A
NM_001031812.3:c.-248+7152G>A	NP_001026982.1:n.-248+7152G>A
NM_001270573.1:c.-48+7152G>A	NP_001257502.1:n.-48+7152G>A
NM_001270574.1:c.-51+7152G>A	NP_001257503.1:n.-51+7152G>A
XM_005271891.1:c.-248+7152G>A	XP_005271948.1:n.-248+7152G>A
XM_005271892.2:c.-248+7152G>A	XP_005271949.1:n.-248+7152G>A
XM_005271893.1:c.-248+7152G>A	XP_005271950.1:n.-248+7152G>A
XM_005271894.2:c.-248+7152G>A	XP_005271951.1:n.-248+7152G>A
XM_005271895.1:c.-248+7152G>A	XP_005271952.1:n.-248+7152G>A
XM_005271896.1:c.-248+7152G>A	XP_005271953.1:n.-248+7152G>A
NM_001364140.1:c.-248+7152G>A	NP_001351069.1:n.-248+7152G>A
NM_001364141.1:c.-333+7152G>A	NP_001351070.1:n.-333+7152G>A
NM_001364143.1:c.-248+7152G>A	NP_001351072.1:n.-248+7152G>A
NM_001364144.1:c.-7+7152G>A	NP_001351073.1:n.-7+7152G>A
NM_001364145.1:c.-7+7152G>A	NP_001351074.1:n.-7+7152G>A
NM_001364146.1:c.-51+7152G>A	NP_001351075.1:n.-51+7152G>A
NM_001364147.1:c.-51+7152G>A	NP_001351076.1:n.-51+7152G>A
NM_001364148.1:c.-51+7152G>A	NP_001351077.1:n.-51+7152G>A
NM_001364149.1:c.-7+7152G>A	NP_001351078.1:n.-7+7152G>A
NM_001364150.1:c.-432+7152G>A	NP_001351079.1:n.-432+7152G>A
XM_005271892.3:c.-248+7152G>A	XP_005271949.1:n.-248+7152G>A
XM_005271894.3:c.-248+7152G>A	XP_005271951.1:n.-248+7152G>A
XM_005271895.3:c.-248+7152G>A	XP_005271952.1:n.-248+7152G>A
XM_017009057.2:c.-248+7152G>A	XP_016864546.1:n.-248+7152G>A
XM_017009059.1:c.-333+7152G>A	XP_016864548.1:n.-333+7152G>A
XM_017009060.1:c.-248+5174G>A	XP_016864549.1:n.-248+5174G>A
XM_017009061.2:c.-248+7152G>A	XP_016864550.1:n.-248+7152G>A
XM_017009063.2:c.-248+7152G>A	XP_016864552.1:n.-248+7152G>A
XM_017009064.2:c.-248+7152G>A	XP_016864553.1:n.-248+7152G>A
XM_017009065.2:c.-248+7152G>A	XP_016864554.1:n.-248+7152G>A
XM_017009067.2:c.-248+7152G>A	XP_016864556.1:n.-248+7152G>A
XM_017009068.2:c.-248+7152G>A	XP_016864557.1:n.-248+7152G>A
XM_017009069.1:c.-333+7152G>A	XP_016864558.1:n.-333+7152G>A
XM_017009070.2:c.-248+7152G>A	XP_016864559.1:n.-248+7152G>A
NM_001270573.2:c.-48+7152G>A	NP_001257502.1:n.-48+7152G>A
NM_001270574.2:c.-51+7152G>A	NP_001257503.1:n.-51+7152G>A
NM_001364140.2:c.-248+7152G>A MANE Select	NP_001351069.1:n.-248+7152G>A
NM_001364141.2:c.-333+7152G>A	NP_001351070.1:n.-333+7152G>A
NM_001364143.2:c.-248+7152G>A	NP_001351072.1:n.-248+7152G>A
NM_001364144.2:c.-7+7152G>A	NP_001351073.1:n.-7+7152G>A
NM_001364145.2:c.-7+7152G>A	NP_001351074.1:n.-7+7152G>A
NM_001364146.2:c.-51+7152G>A	NP_001351075.1:n.-51+7152G>A
NM_001364147.2:c.-51+7152G>A	NP_001351076.1:n.-51+7152G>A
NM_001364148.2:c.-51+7152G>A	NP_001351077.1:n.-51+7152G>A
NM_001364149.2:c.-7+7152G>A	NP_001351078.1:n.-7+7152G>A
NM_001364150.2:c.-432+7152G>A	NP_001351079.1:n.-432+7152G>A
NM_001031812.4:c.-248+7152G>A	NP_001026982.1:n.-248+7152G>A
NM_004384.5:c.-248+7152G>A	NP_004375.2:n.-248+7152G>A