Canonical Allele Identifier: CA799186088

Gene: HPSE

Linked Data

• dbSNP Id: rs4693608
• MyVariant Identifiers: chr4:g.84241357G>C (hg19) ; chr4:g.83320204G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.83320204G>C , CM000666.2:g.83320204G>C	GRCh38
NC_000004.11:g.84241357G>C , CM000666.1:g.84241357G>C	GRCh37
NC_000004.10:g.84460381G>C	NCBI36
NG_028037.1:g.19950C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000311412.10:c.374-735C>G MANE Select	ENSP00000308107.5:n.374-735C>G
ENST00000680713.1:n.393-735C>G
ENST00000681769.1:c.374-735C>G	ENSP00000506434.1:n.374-735C>G
ENST00000311412.9:c.374-735C>G	ENSP00000308107.5:n.374-735C>G
ENST00000405413.6:c.374-735C>G	ENSP00000384262.2:n.374-735C>G
ENST00000507150.5:c.374-735C>G	ENSP00000426139.1:n.374-735C>G
ENST00000508891.5:c.374-735C>G	ENSP00000421827.1:n.374-735C>G
ENST00000509906.5:c.374-735C>G	ENSP00000421038.1:n.374-735C>G
ENST00000512196.5:c.374-735C>G	ENSP00000423265.1:n.374-735C>G
ENST00000513463.1:c.374-735C>G	ENSP00000421365.1:n.374-735C>G
NM_001098540.2:c.374-735C>G	NP_001092010.1:n.374-735C>G
NM_001166498.2:c.374-735C>G	NP_001159970.1:n.374-735C>G
NM_001199830.1:c.374-735C>G	NP_001186759.1:n.374-735C>G
NM_006665.5:c.374-735C>G	NP_006656.2:n.374-735C>G
NM_001098540.3:c.374-735C>G MANE Select	NP_001092010.1:n.374-735C>G
NM_001166498.3:c.374-735C>G	NP_001159970.1:n.374-735C>G
NM_006665.6:c.374-735C>G	NP_006656.2:n.374-735C>G