Canonical Allele Identifier: CA363849332

Gene: PI16

Linked Data

• MyVariant Identifiers: chr6:g.36922585C>A (hg19) ; chr6:g.36954809C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36954809C>A , CM000668.2:g.36954809C>A	GRCh38
NC_000006.11:g.36922585C>A , CM000668.1:g.36922585C>A	GRCh37
NC_000006.10:g.37030563C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373674.4:c.49C>A MANE Select	ENSP00000362778.3:p.Leu17Met
ENST00000647861.1:c.49C>A	ENSP00000497550.1:p.Leu17Met
ENST00000373674.3:c.49C>A	ENSP00000362778.3:p.Leu17Met
ENST00000611814.4:c.49C>A	ENSP00000478888.1:p.Leu17Met
NM_001199159.1:c.49C>A	NP_001186088.1:p.Leu17Met
NM_153370.2:c.49C>A	NP_699201.2:p.Leu17Met
XM_005248917.1:c.49C>A	XP_005248974.1:p.Leu17Met
XM_011514375.1:c.49C>A	XP_011512677.1:p.Leu17Met
XM_005248917.3:c.49C>A	XP_005248974.1:p.Leu17Met
XM_011514375.3:c.49C>A	XP_011512677.1:p.Leu17Met
XM_017010430.2:c.49C>A	XP_016865919.1:p.Leu17Met
NM_153370.3:c.49C>A MANE Select	NP_699201.2:p.Leu17Met
NM_001199159.2:c.49C>A	NP_001186088.1:p.Leu17Met