Canonical Allele Identifier: CA411667828

Gene: TNRC6B

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40312911C>G , CM000684.2:g.40312911C>G	GRCh38
NC_000022.10:g.40708915C>G , CM000684.1:g.40708915C>G	GRCh37
NC_000022.9:g.39038861C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001162501.2:c.4592C>G MANE Select	NP_001155973.1:p.Ser1531Cys
ENST00000454349.7:c.4592C>G MANE Select	ENSP00000401946.2:p.Ser1531Cys
NM_001024843.1:c.2180C>G	NP_001020014.1:p.Ser727Cys
NM_001024843.2:c.2180C>G	NP_001020014.1:p.Ser727Cys
NM_001162501.1:c.4592C>G	NP_001155973.1:p.Ser1531Cys
NM_015088.2:c.4262C>G	NP_055903.2:p.Ser1421Cys
NM_015088.3:c.4262C>G	NP_055903.2:p.Ser1421Cys
ENST00000301923.13:c.2180C>G	ENSP00000306759.9:p.Ser727Cys
ENST00000335727.13:c.4262C>G	ENSP00000338371.8:p.Ser1421Cys
ENST00000402203.5:c.2180C>G	ENSP00000384795.1:p.Ser727Cys
ENST00000446273.1:c.3649C>G
ENST00000454349.6:c.4592C>G	ENSP00000401946.2:p.Ser1531Cys