Canonical Allele Identifier: CA2499214682

Gene: TMEM222

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.27334277_27334279del , CM000663.2:g.27334277_27334279del	GRCh38
NC_000001.10:g.27660768_27660770del , CM000663.1:g.27660768_27660770del	GRCh37
NC_000001.9:g.27533355_27533357del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032125.3:c.535_537del MANE Select	NP_115501.2:p.Val179del
ENST00000374076.9:c.535_537del MANE Select	ENSP00000363189.4:p.Val179del
NM_032125.2:c.535_537del	NP_115501.2:p.Val179del
NR_037576.1:n.741_743del
NR_037576.2:n.641_643del
NR_037577.1:n.588_590del
NR_037577.2:n.488_490del
NR_037580.1:n.741_743del
NR_037580.2:n.641_643del
ENST00000374076.8:c.535_537del	ENSP00000363189.4:p.Val179del
ENST00000464720.5:c.*370_*372del	ENSP00000419528.2:n.*370_*372del
ENST00000464813.5:c.436_438del	ENSP00000417853.2:p.Val146del
ENST00000470223.1:n.719_721del
ENST00000471456.1:n.1836_1838del
ENST00000478104.5:c.436_438del	ENSP00000417603.2:p.Val146del
ENST00000486082.5:c.*370_*372del	ENSP00000417720.2:n.*370_*372del
ENST00000498220.1:c.508_510del	ENSP00000419292.1:p.Val170del
ENST00000608611.5:c.436_438del	ENSP00000476439.1:p.Val146del
ENST00000611517.4:c.535_537del	ENSP00000483276.1:p.Val179del