Canonical Allele Identifier: CA370667925

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37630389A>T (hg19) ; chr8:g.37772871A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37772871A>T , CM000670.2:g.37772871A>T	GRCh38
NC_000008.10:g.37630389A>T , CM000670.1:g.37630389A>T	GRCh37
NC_000008.9:g.37749547A>T	NCBI36
NG_053030.1:g.16119A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.436A>T MANE Select	ENSP00000333551.3:p.Asn146Tyr
ENST00000328195.7:c.436A>T	ENSP00000333551.3:p.Asn146Tyr
ENST00000521631.1:n.119A>T
ENST00000523187.5:c.280A>T	ENSP00000427886.1:p.Asn94Tyr
ENST00000523358.5:c.436A>T	ENSP00000427778.1:p.Asn146Tyr
ENST00000523521.1:c.193A>T	ENSP00000429425.1:p.Asn65Tyr
NM_007198.3:c.436A>T	NP_009129.1:p.Asn146Tyr
NM_001349346.1:c.436A>T	NP_001336275.1:p.Asn146Tyr
NM_001349347.1:c.430A>T	NP_001336276.1:p.Asn144Tyr
NM_001349348.1:c.280A>T	NP_001336277.1:p.Asn94Tyr
NM_007198.4:c.436A>T MANE Select	NP_009129.1:p.Asn146Tyr
NM_001349346.2:c.436A>T	NP_001336275.1:p.Asn146Tyr
NM_001349347.2:c.430A>T	NP_001336276.1:p.Asn144Tyr
NM_001349348.2:c.280A>T	NP_001336277.1:p.Asn94Tyr