Canonical Allele Identifier: CA1272520788

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250919_96250920delinsTA , CM000664.2:g.96250919_96250920delinsTA	GRCh38
NC_000002.11:g.96916657_96916658delinsTA , CM000664.1:g.96916657_96916658delinsTA	GRCh37
NC_000002.10:g.96280384_96280385delinsTA	NCBI36
NG_027695.1:g.20094_20095delinsTA , LRG_528:g.20094_20095delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2888_*2889delinsTA MANE Select	ENSP00000258439.3:n.*2888_*2889delinsTA
ENST00000258439.7:c.*2888_*2889delinsTA	ENSP00000258439.2:n.*2888_*2889delinsTA
NM_001193304.2:c.*2888_*2889delinsTA	NP_001180233.1:n.*2888_*2889delinsTA
NM_017849.3:c.*2888_*2889delinsTA , LRG_528t1:c.*2888_*2889delinsTA	NP_060319.1:n.*2888_*2889delinsTA
XM_017004450.1:c.*2189_*2190delinsTA	XP_016859939.1:n.*2189_*2190delinsTA
XM_017004452.1:c.*2888_*2889delinsTA	XP_016859941.1:n.*2888_*2889delinsTA
NM_001193304.3:c.*2888_*2889delinsTA	NP_001180233.1:n.*2888_*2889delinsTA
NM_017849.4:c.*2888_*2889delinsTA MANE Select	NP_060319.1:n.*2888_*2889delinsTA