Canonical Allele Identifier: CA1272520989

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251347_96251349delinsGTC , CM000664.2:g.96251347_96251349delinsGTC	GRCh38
NC_000002.11:g.96917085_96917087delinsGTC , CM000664.1:g.96917085_96917087delinsGTC	GRCh37
NC_000002.10:g.96280812_96280814delinsGTC	NCBI36
NG_027695.1:g.19665_19667delinsGAC , LRG_528:g.19665_19667delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2459_*2461delinsGAC MANE Select	ENSP00000258439.3:n.*2459_*2461delinsGAC
ENST00000258439.7:c.*2459_*2461delinsGAC	ENSP00000258439.2:n.*2459_*2461delinsGAC
NM_001193304.2:c.*2459_*2461delinsGAC	NP_001180233.1:n.*2459_*2461delinsGAC
NM_017849.3:c.*2459_*2461delinsGAC , LRG_528t1:c.*2459_*2461delinsGAC	NP_060319.1:n.*2459_*2461delinsGAC
XM_017004450.1:c.*1760_*1762delinsGAC	XP_016859939.1:n.*1760_*1762delinsGAC
XM_017004452.1:c.*2459_*2461delinsGAC	XP_016859941.1:n.*2459_*2461delinsGAC
NM_001193304.3:c.*2459_*2461delinsGAC	NP_001180233.1:n.*2459_*2461delinsGAC
NM_017849.4:c.*2459_*2461delinsGAC MANE Select	NP_060319.1:n.*2459_*2461delinsGAC