Canonical Allele Identifier: CA2338415896

Gene: PPP1R13L

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45404702A= , CM000681.2:g.45404702A=	GRCh38
NC_000019.9:g.45907960A= , CM000681.1:g.45907960A=	GRCh37
NC_000019.8:g.50599800A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006663.4:c.-22+297T= MANE Select	NP_006654.2:n.-22+297T=
ENST00000360957.10:c.-22+297T= MANE Select	ENSP00000354218.4:n.-22+297T=
NM_001142502.1:c.-22+1590T=	NP_001135974.1:n.-22+1590T=
NM_001142502.2:c.-22+1590T=	NP_001135974.1:n.-22+1590T=
NM_006663.3:c.-22+297T=	NP_006654.2:n.-22+297T=
ENST00000360957.9:c.-22+297T=	ENSP00000354218.4:n.-22+297T=
ENST00000418234.6:c.-22+1590T=	ENSP00000403902.1:n.-22+1590T=
ENST00000585905.1:n.18+1590T=
ENST00000592134.1:c.-148+297T=	ENSP00000467471.1:n.-148+297T=
ENST00000593226.5:c.-22+297T=	ENSP00000466730.1:n.-22+297T=
XM_017026177.1:c.-22+297T=	XP_016881666.1:n.-22+297T=
XM_017026178.1:c.-148+1590T=	XP_016881667.1:n.-148+1590T=
XM_017026179.1:c.-22+1590T=	XP_016881668.1:n.-22+1590T=