Canonical Allele Identifier: CA2577034259

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96255066_96255068del , CM000664.2:g.96255066_96255068del	GRCh38
NC_000002.11:g.96920804_96920806del , CM000664.1:g.96920804_96920806del	GRCh37
NC_000002.10:g.96284531_96284533del	NCBI36
NG_027695.1:g.15948_15950del , LRG_528:g.15948_15950del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.245-69_245-67del MANE Select	ENSP00000258439.3:n.245-69_245-67del
ENST00000258439.7:c.245-69_245-67del	ENSP00000258439.2:n.245-69_245-67del
ENST00000432959.1:c.245-69_245-67del	ENSP00000416660.1:n.245-69_245-67del
ENST00000435268.1:c.-8-69_-8-67del	ENSP00000411810.1:n.-8-69_-8-67del
NM_001193304.2:c.245-69_245-67del	NP_001180233.1:n.245-69_245-67del
NM_017849.3:c.245-69_245-67del , LRG_528t1:c.245-69_245-67del	NP_060319.1:n.245-69_245-67del
XM_017004450.1:c.-674-69_-674-67del	XP_016859939.1:n.-674-69_-674-67del
XM_017004452.1:c.-8-69_-8-67del	XP_016859941.1:n.-8-69_-8-67del
NM_001193304.3:c.245-69_245-67del	NP_001180233.1:n.245-69_245-67del
NM_017849.4:c.245-69_245-67del MANE Select	NP_060319.1:n.245-69_245-67del