Canonical Allele Identifier: CA370666864

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37623257A>C (hg19) ; chr8:g.37765739A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765739A>C , CM000670.2:g.37765739A>C	GRCh38
NC_000008.10:g.37623257A>C , CM000670.1:g.37623257A>C	GRCh37
NC_000008.9:g.37742415A>C	NCBI36
NG_053030.1:g.8987A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000328195.8:c.236A>C MANE Select	ENSP00000333551.3:p.Asn79Thr
ENST00000328195.7:c.236A>C	ENSP00000333551.3:p.Asn79Thr
ENST00000518036.5:c.*88A>C	ENSP00000428005.1:n.*88A>C
ENST00000520073.5:n.301A>C
ENST00000523187.5:c.80A>C	ENSP00000427886.1:p.Asn27Thr
ENST00000523358.5:c.236A>C	ENSP00000427778.1:p.Asn79Thr
ENST00000523994.1:n.241A>C
NM_007198.3:c.236A>C	NP_009129.1:p.Asn79Thr
NM_001349346.1:c.236A>C	NP_001336275.1:p.Asn79Thr
NM_001349347.1:c.230A>C	NP_001336276.1:p.Asn77Thr
NM_001349348.1:c.80A>C	NP_001336277.1:p.Asn27Thr
NM_001349349.1:c.341A>C	NP_001336278.1:p.Asn114Thr
NM_007198.4:c.236A>C MANE Select	NP_009129.1:p.Asn79Thr
NM_001349346.2:c.236A>C	NP_001336275.1:p.Asn79Thr
NM_001349347.2:c.230A>C	NP_001336276.1:p.Asn77Thr
NM_001349348.2:c.80A>C	NP_001336277.1:p.Asn27Thr