Canonical Allele Identifier: CA370667933

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37630392A>T (hg19) ; chr8:g.37772874A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37772874A>T , CM000670.2:g.37772874A>T	GRCh38
NC_000008.10:g.37630392A>T , CM000670.1:g.37630392A>T	GRCh37
NC_000008.9:g.37749550A>T	NCBI36
NG_053030.1:g.16122A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.439A>T MANE Select	ENSP00000333551.3:p.Thr147Ser
ENST00000328195.7:c.439A>T	ENSP00000333551.3:p.Thr147Ser
ENST00000521631.1:n.122A>T
ENST00000523187.5:c.283A>T	ENSP00000427886.1:p.Thr95Ser
ENST00000523358.5:c.439A>T	ENSP00000427778.1:p.Thr147Ser
ENST00000523521.1:c.196A>T	ENSP00000429425.1:p.Thr66Ser
NM_007198.3:c.439A>T	NP_009129.1:p.Thr147Ser
NM_001349346.1:c.439A>T	NP_001336275.1:p.Thr147Ser
NM_001349347.1:c.433A>T	NP_001336276.1:p.Thr145Ser
NM_001349348.1:c.283A>T	NP_001336277.1:p.Thr95Ser
NM_007198.4:c.439A>T MANE Select	NP_009129.1:p.Thr147Ser
NM_001349346.2:c.439A>T	NP_001336275.1:p.Thr147Ser
NM_001349347.2:c.433A>T	NP_001336276.1:p.Thr145Ser
NM_001349348.2:c.283A>T	NP_001336277.1:p.Thr95Ser