Canonical Allele Identifier: CA1272521183

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251772_96251775delinsAAAG , CM000664.2:g.96251772_96251775delinsAAAG	GRCh38
NC_000002.11:g.96917510_96917513delinsAAAG , CM000664.1:g.96917510_96917513delinsAAAG	GRCh37
NC_000002.10:g.96281237_96281240delinsAAAG	NCBI36
NG_027695.1:g.19239_19242delinsCTTT , LRG_528:g.19239_19242delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2033_*2036delinsCTTT MANE Select	ENSP00000258439.3:n.*2033_*2036delinsCTTT
ENST00000258439.7:c.*2033_*2036delinsCTTT	ENSP00000258439.2:n.*2033_*2036delinsCTTT
ENST00000432959.1:c.*2033_*2036delinsCTTT	ENSP00000416660.1:n.*2033_*2036delinsCTTT
NM_001193304.2:c.*2033_*2036delinsCTTT	NP_001180233.1:n.*2033_*2036delinsCTTT
NM_017849.3:c.*2033_*2036delinsCTTT , LRG_528t1:c.*2033_*2036delinsCTTT	NP_060319.1:n.*2033_*2036delinsCTTT
XM_017004450.1:c.*1334_*1337delinsCTTT	XP_016859939.1:n.*1334_*1337delinsCTTT
XM_017004452.1:c.*2033_*2036delinsCTTT	XP_016859941.1:n.*2033_*2036delinsCTTT
NM_001193304.3:c.*2033_*2036delinsCTTT	NP_001180233.1:n.*2033_*2036delinsCTTT
NM_017849.4:c.*2033_*2036delinsCTTT MANE Select	NP_060319.1:n.*2033_*2036delinsCTTT