Canonical Allele Identifier: CA2788891762

Gene: PAPSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727148_87727150dup , CM000672.2:g.87727148_87727150dup	GRCh38
NC_000010.10:g.89486905_89486907dup , CM000672.1:g.89486905_89486907dup	GRCh37
NC_000010.9:g.89476885_89476887dup	NCBI36
NG_012150.1:g.72430_72432dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.881-136_881-134dup MANE Select	ENSP00000406157.1:n.881-136_881-134dup
ENST00000361175.8:c.866-136_866-134dup	ENSP00000354436.4:n.866-136_866-134dup
ENST00000456849.1:c.881-136_881-134dup	ENSP00000406157.1:n.881-136_881-134dup
NM_001015880.1:c.881-136_881-134dup	NP_001015880.1:n.881-136_881-134dup
NM_004670.3:c.866-136_866-134dup	NP_004661.2:n.866-136_866-134dup
NM_001015880.2:c.881-136_881-134dup MANE Select	NP_001015880.1:n.881-136_881-134dup
NM_004670.4:c.866-136_866-134dup	NP_004661.2:n.866-136_866-134dup