Canonical Allele Identifier: CA1272520727

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250795_96250797delinsCTA , CM000664.2:g.96250795_96250797delinsCTA	GRCh38
NC_000002.11:g.96916533_96916535delinsCTA , CM000664.1:g.96916533_96916535delinsCTA	GRCh37
NC_000002.10:g.96280260_96280262delinsCTA	NCBI36
NG_027695.1:g.20217_20219delinsTAG , LRG_528:g.20217_20219delinsTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*3011_*3013delinsTAG MANE Select	ENSP00000258439.3:n.*3011_*3013delinsTAG
ENST00000258439.7:c.*3011_*3013delinsTAG	ENSP00000258439.2:n.*3011_*3013delinsTAG
NM_001193304.2:c.*3011_*3013delinsTAG	NP_001180233.1:n.*3011_*3013delinsTAG
NM_017849.3:c.*3011_*3013delinsTAG , LRG_528t1:c.*3011_*3013delinsTAG	NP_060319.1:n.*3011_*3013delinsTAG
XM_017004450.1:c.*2312_*2314delinsTAG	XP_016859939.1:n.*2312_*2314delinsTAG
XM_017004452.1:c.*3011_*3013delinsTAG	XP_016859941.1:n.*3011_*3013delinsTAG
NM_001193304.3:c.*3011_*3013delinsTAG	NP_001180233.1:n.*3011_*3013delinsTAG
NM_017849.4:c.*3011_*3013delinsTAG MANE Select	NP_060319.1:n.*3011_*3013delinsTAG