Canonical Allele Identifier: CA1777240069

Gene: PLPBP

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37772859A= , CM000670.2:g.37772859A=	GRCh38
NC_000008.10:g.37630377A= , CM000670.1:g.37630377A=	GRCh37
NC_000008.9:g.37749535A=	NCBI36
NG_053030.1:g.16107A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.424A= MANE Select	ENSP00000333551.3:p.Met142=
ENST00000328195.7:c.424A=	ENSP00000333551.3:p.Met142=
ENST00000518036.5:c.*276A=	ENSP00000428005.1:n.*276A=
ENST00000521631.1:n.107A=
ENST00000523187.5:c.268A=	ENSP00000427886.1:p.Met90=
ENST00000523358.5:c.424A=	ENSP00000427778.1:p.Met142=
ENST00000523521.1:c.181A=	ENSP00000429425.1:p.Met61=
NM_007198.3:c.424A=	NP_009129.1:p.Met142=
NM_001349346.1:c.424A=	NP_001336275.1:p.Met142=
NM_001349347.1:c.418A=	NP_001336276.1:p.Met140=
NM_001349348.1:c.268A=	NP_001336277.1:p.Met90=
NM_007198.4:c.424A= MANE Select	NP_009129.1:p.Met142=
NM_001349346.2:c.424A=	NP_001336275.1:p.Met142=
NM_001349347.2:c.418A=	NP_001336276.1:p.Met140=
NM_001349348.2:c.268A=	NP_001336277.1:p.Met90=