Canonical Allele Identifier: CA400141255

Gene: PHB1

Linked Data

• MyVariant Identifiers: chr17:g.47486459T>G (hg19) ; chr17:g.49409097T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49409097T>G , CM000679.2:g.49409097T>G	GRCh38
NC_000017.10:g.47486459T>G , CM000679.1:g.47486459T>G	GRCh37
NC_000017.9:g.44841458T>G	NCBI36
NG_023046.1:g.10784A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696365.1:c.417+38A>C	ENSP00000512581.1:n.417+38A>C
ENST00000300408.8:c.455A>C MANE Select	ENSP00000300408.3:p.Asp152Ala
ENST00000419140.7:c.455A>C	ENSP00000393320.3:p.Asp152Ala
ENST00000434917.3:n.546A>C
ENST00000446735.6:c.293A>C	ENSP00000407828.2:p.Asp98Ala
ENST00000504124.6:c.455A>C	ENSP00000426433.3:p.Asp152Ala
ENST00000508009.6:n.546A>C
ENST00000511832.6:c.455A>C	ENSP00000425035.2:p.Asp152Ala
ENST00000512041.7:c.455A>C	ENSP00000422182.3:p.Asp152Ala
ENST00000614445.5:c.455A>C	ENSP00000479488.1:p.Asp152Ala
ENST00000617874.5:c.455A>C	ENSP00000484113.1:p.Asp152Ala
ENST00000300408.7:c.455A>C	ENSP00000300408.3:p.Asp152Ala
ENST00000393345.8:n.506A>C
ENST00000419140.6:c.455A>C	ENSP00000393320.2:p.Asp152Ala
ENST00000446735.5:c.455A>C	ENSP00000407828.1:p.Asp152Ala
ENST00000504124.5:c.455A>C	ENSP00000426433.2:p.Asp152Ala
ENST00000506273.1:n.410A>C
ENST00000508009.5:n.282A>C
ENST00000511832.5:c.417+38A>C	ENSP00000425035.1:n.417+38A>C
ENST00000512041.6:c.455A>C	ENSP00000422182.2:p.Asp152Ala
ENST00000614445.4:c.455A>C	ENSP00000479488.1:p.Asp152Ala
ENST00000617874.4:c.455A>C	ENSP00000484113.1:p.Asp152Ala
NM_001281496.1:c.455A>C	NP_001268425.1:p.Asp152Ala
NM_001281497.1:c.417+38A>C	NP_001268426.1:n.417+38A>C
NM_001281715.1:c.455A>C	NP_001268644.1:p.Asp152Ala
NM_002634.3:c.455A>C	NP_002625.1:p.Asp152Ala
XM_017024763.1:c.455A>C	XP_016880252.1:p.Asp152Ala
NM_002634.4:c.455A>C MANE Select	NP_002625.1:p.Asp152Ala
NM_001281496.2:c.455A>C	NP_001268425.1:p.Asp152Ala
NM_001281497.2:c.417+38A>C	NP_001268426.1:n.417+38A>C
NM_001281715.2:c.455A>C	NP_001268644.1:p.Asp152Ala