Canonical Allele Identifier: CA366857332

Gene: TMEM106B

Linked Data

• MyVariant Identifiers: chr7:g.12269439G>A (hg19) ; chr7:g.12229813G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.12229813G>A , CM000669.2:g.12229813G>A	GRCh38
NC_000007.13:g.12269439G>A , CM000669.1:g.12269439G>A	GRCh37
NC_000007.12:g.12235964G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000444443.6:c.576G>A	ENSP00000401302.2:p.Met192Ile
ENST00000704347.1:c.282-576G>A	ENSP00000515858.1:n.282-576G>A
ENST00000704348.1:c.442-576G>A	ENSP00000515859.1:n.442-576G>A
ENST00000704349.1:c.442-576G>A	ENSP00000515860.1:n.442-576G>A
ENST00000704416.1:c.282G>A	ENSP00000515892.1:p.Met94Ile
ENST00000704417.1:c.501G>A	ENSP00000515893.1:p.Met167Ile
ENST00000704455.1:c.576G>A	ENSP00000515905.1:p.Met192Ile
ENST00000704457.1:c.576G>A	ENSP00000515907.1:p.Met192Ile
ENST00000396668.8:c.576G>A MANE Select	ENSP00000379902.3:p.Met192Ile
ENST00000396667.7:c.576G>A	ENSP00000379901.2:p.Met192Ile
ENST00000396668.7:c.576G>A	ENSP00000379902.3:p.Met192Ile
ENST00000420833.5:c.*462G>A	ENSP00000391016.1:n.*462G>A
ENST00000492762.1:n.66G>A
NM_001134232.1:c.576G>A	NP_001127704.1:p.Met192Ile
NM_018374.3:c.576G>A	NP_060844.2:p.Met192Ile
XM_005249789.1:c.576G>A	XP_005249846.1:p.Met192Ile
NM_001134232.2:c.576G>A MANE Select	NP_001127704.1:p.Met192Ile
NM_018374.4:c.576G>A	NP_060844.2:p.Met192Ile