Canonical Allele Identifier: CA1472759720

Gene: HPSE

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.83309479G= , CM000666.2:g.83309479G=	GRCh38
NC_000004.11:g.84230632G= , CM000666.1:g.84230632G=	GRCh37
NC_000004.10:g.84449656G=	NCBI36
NG_028037.1:g.30675C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311412.10:c.907C= MANE Select	ENSP00000308107.5:p.Arg303=
ENST00000681769.1:c.907C=	ENSP00000506434.1:p.Arg303=
ENST00000311412.9:c.907C=	ENSP00000308107.5:p.Arg303=
ENST00000405413.6:c.907C=	ENSP00000384262.2:p.Arg303=
ENST00000507150.5:c.*57C=	ENSP00000426139.1:n.*57C=
ENST00000508891.5:c.*57C=	ENSP00000421827.1:n.*57C=
ENST00000509906.5:c.907C=	ENSP00000421038.1:p.Arg303=
ENST00000512196.5:c.907C=	ENSP00000423265.1:p.Arg303=
ENST00000513463.1:c.733C=	ENSP00000421365.1:p.Arg245=
NM_001098540.2:c.907C=	NP_001092010.1:p.Arg303=
NM_001166498.2:c.907C=	NP_001159970.1:p.Arg303=
NM_001199830.1:c.733C=	NP_001186759.1:p.Arg245=
NM_006665.5:c.907C=	NP_006656.2:p.Arg303=
XR_938943.1:n.100-6969G=
NM_001098540.3:c.907C= MANE Select	NP_001092010.1:p.Arg303=
NM_001166498.3:c.907C=	NP_001159970.1:p.Arg303=
NM_006665.6:c.907C=	NP_006656.2:p.Arg303=