Canonical Allele Identifier: CA2586964989

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254082_96254084del , CM000664.2:g.96254082_96254084del	GRCh38
NC_000002.11:g.96919820_96919822del , CM000664.1:g.96919820_96919822del	GRCh37
NC_000002.10:g.96283547_96283549del	NCBI36
NG_027695.1:g.16932_16934del , LRG_528:g.16932_16934del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.443_445del MANE Select	ENSP00000258439.3:p.Tyr148del
ENST00000258439.7:c.443_445del	ENSP00000258439.2:p.Tyr148del
ENST00000432959.1:c.443_445del	ENSP00000416660.1:p.Tyr148del
ENST00000435268.1:c.191_193del	ENSP00000411810.1:p.Tyr64del
NM_001193304.2:c.443_445del	NP_001180233.1:p.Tyr148del
NM_017849.3:c.443_445del , LRG_528t1:c.443_445del	NP_060319.1:p.Tyr148del
XM_017004450.1:c.-476_-474del	XP_016859939.1:n.-476_-474del
XM_017004452.1:c.191_193del	XP_016859941.1:p.Tyr64del
NM_001193304.3:c.443_445del	NP_001180233.1:p.Tyr148del
NM_017849.4:c.443_445del MANE Select	NP_060319.1:p.Tyr148del