Canonical Allele Identifier: CA11693062

Gene: HPSE

Linked Data

• ClinVar Variation Id: 1235597
• ClinVar RCV Id: RCV001618138
• dbSNP Id: rs4693608
• gnomAD v2: 4-84241357-G-A
• gnomAD v3: 4-83320204-G-A
• gnomAD v4: 4-83320204-G-A
• MyVariant Identifiers: chr4:g.84241357G>A (hg19) ; chr4:g.83320204G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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