Canonical Allele Identifier: CA2678516998

Gene: PI16

Linked Data

• gnomAD v4: 6-36954912-CCTCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36954913_36954916del , CM000668.2:g.36954913_36954916del	GRCh38
NC_000006.11:g.36922689_36922692del , CM000668.1:g.36922689_36922692del	GRCh37
NC_000006.10:g.37030667_37030670del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373674.4:c.153_156del MANE Select	ENSP00000362778.3:p.Ser52ThrfsTer5
ENST00000647861.1:c.153_156del	ENSP00000497550.1:p.Ser52ThrfsTer5
ENST00000373674.3:c.153_156del	ENSP00000362778.3:p.Ser52ThrfsTer5
ENST00000611814.4:c.153_156del	ENSP00000478888.1:p.Ser52ThrfsTer5
NM_001199159.1:c.153_156del	NP_001186088.1:p.Ser52ThrfsTer5
NM_153370.2:c.153_156del	NP_699201.2:p.Ser52ThrfsTer5
XM_005248917.1:c.153_156del	XP_005248974.1:p.Ser52ThrfsTer5
XM_011514375.1:c.153_156del	XP_011512677.1:p.Ser52ThrfsTer5
XM_005248917.3:c.153_156del	XP_005248974.1:p.Ser52ThrfsTer5
XM_011514375.3:c.153_156del	XP_011512677.1:p.Ser52ThrfsTer5
XM_017010430.2:c.153_156del	XP_016865919.1:p.Ser52ThrfsTer5
NM_153370.3:c.153_156del MANE Select	NP_699201.2:p.Ser52ThrfsTer5
NM_001199159.2:c.153_156del	NP_001186088.1:p.Ser52ThrfsTer5