Canonical Allele Identifier: CA366857334

Gene: TMEM106B

Linked Data

• gnomAD v4: 7-12229813-G-T
• MyVariant Identifiers: chr7:g.12269439G>T (hg19) ; chr7:g.12229813G>T (hg38)

Genomic Alleles

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

Transcript Alleles

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