Canonical Allele Identifier: CA1407094951

Gene: PLS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142712185A= , CM000665.2:g.142712185A=	GRCh38
NC_000003.11:g.142431027A= , CM000665.1:g.142431027A=	GRCh37
NC_000003.10:g.143913717A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000457734.7:c.*178A= MANE Select	ENSP00000387890.2:n.*178A=
ENST00000337777.7:c.*178A=	ENSP00000336831.3:n.*178A=
ENST00000457734.6:c.*178A=	ENSP00000387890.2:n.*178A=
NM_001145319.1:c.*178A=	NP_001138791.1:n.*178A=
NM_001172312.1:c.*178A=	NP_001165783.1:n.*178A=
NM_002670.2:c.*178A=	NP_002661.2:n.*178A=
XM_006713660.2:c.*178A=	XP_006713723.1:n.*178A=
XM_011512900.1:c.*178A=	XP_011511202.1:n.*178A=
XM_011512901.1:c.*178A=	XP_011511203.1:n.*178A=
XM_011512902.1:c.*178A=	XP_011511204.1:n.*178A=
XM_011512903.1:c.*178A=	XP_011511205.1:n.*178A=
XM_006713660.3:c.*178A=	XP_006713723.1:n.*178A=
XM_011512900.2:c.*178A=	XP_011511202.1:n.*178A=
XM_011512903.2:c.*178A=	XP_011511205.1:n.*178A=
XM_017006626.1:c.*178A=	XP_016862115.1:n.*178A=
XM_017006627.1:c.*178A=	XP_016862116.1:n.*178A=
NM_001145319.2:c.*178A= MANE Select	NP_001138791.1:n.*178A=
NM_002670.3:c.*178A=	NP_002661.2:n.*178A=
NM_001172312.2:c.*178A=	NP_001165783.1:n.*178A=