Canonical Allele Identifier: CA2610038238
Gene: PAPSS2 HGNC NCBI

Linked Data

gnomAD v4: 10-87727250-C-CTAA
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727252_87727253insATA , CM000672.2:g.87727252_87727253insATA GRCh38
NC_000010.10:g.89487009_89487010insATA , CM000672.1:g.89487009_89487010insATA GRCh37
NC_000010.9:g.89476989_89476990insATA NCBI36
NG_012150.1:g.72534_72535insATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.881-32_881-31insATA MANE Select ENSP00000406157.1:n.881-32_881-31insATA
ENST00000361175.8:c.866-32_866-31insATA ENSP00000354436.4:n.866-32_866-31insATA
ENST00000456849.1:c.881-32_881-31insATA ENSP00000406157.1:n.881-32_881-31insATA
NM_001015880.1:c.881-32_881-31insATA NP_001015880.1:n.881-32_881-31insATA
NM_004670.3:c.866-32_866-31insATA NP_004661.2:n.866-32_866-31insATA
NM_001015880.2:c.881-32_881-31insATA MANE Select NP_001015880.1:n.881-32_881-31insATA
NM_004670.4:c.866-32_866-31insATA NP_004661.2:n.866-32_866-31insATA
Search 100 bp 5'
Search 100 bp 3'