Canonical Allele Identifier: CA2660177634

Gene: TMEM127

Linked Data

• gnomAD v4: 2-96254231-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254235del , CM000664.2:g.96254235del	GRCh38
NC_000002.11:g.96919973del , CM000664.1:g.96919973del	GRCh37
NC_000002.10:g.96283700del	NCBI36
NG_027695.1:g.16782del , LRG_528:g.16782del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.410-117del MANE Select	ENSP00000258439.3:n.410-117del
ENST00000258439.7:c.410-117del	ENSP00000258439.2:n.410-117del
ENST00000432959.1:c.410-117del	ENSP00000416660.1:n.410-117del
ENST00000435268.1:c.158-117del	ENSP00000411810.1:n.158-117del
NM_001193304.2:c.410-117del	NP_001180233.1:n.410-117del
NM_017849.3:c.410-117del , LRG_528t1:c.410-117del	NP_060319.1:n.410-117del
XM_017004450.1:c.-509-117del	XP_016859939.1:n.-509-117del
XM_017004452.1:c.158-117del	XP_016859941.1:n.158-117del
NM_001193304.3:c.410-117del	NP_001180233.1:n.410-117del
NM_017849.4:c.410-117del MANE Select	NP_060319.1:n.410-117del