Canonical Allele Identifier: CA1272520683

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250706_96250710delinsTGAAG , CM000664.2:g.96250706_96250710delinsTGAAG	GRCh38
NC_000002.11:g.96916444_96916448delinsTGAAG , CM000664.1:g.96916444_96916448delinsTGAAG	GRCh37
NC_000002.10:g.96280171_96280175delinsTGAAG	NCBI36
NG_027695.1:g.20304_20308delinsCTTCA , LRG_528:g.20304_20308delinsCTTCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*3098_*3102delinsCTTCA MANE Select	ENSP00000258439.3:n.*3098_*3102delinsCTTC...
ENST00000258439.7:c.*3098_*3102delinsCTTCA	ENSP00000258439.2:n.*3098_*3102delinsCTTC...
NM_001193304.2:c.*3098_*3102delinsCTTCA	NP_001180233.1:n.*3098_*3102delinsCTTCA
NM_017849.3:c.*3098_*3102delinsCTTCA , LRG_528t1:c.*3098_*3102delinsCTTCA	NP_060319.1:n.*3098_*3102delinsCTTCA
XM_017004450.1:c.*2399_*2403delinsCTTCA	XP_016859939.1:n.*2399_*2403delinsCTTCA
XM_017004452.1:c.*3098_*3102delinsCTTCA	XP_016859941.1:n.*3098_*3102delinsCTTCA
NM_001193304.3:c.*3098_*3102delinsCTTCA	NP_001180233.1:n.*3098_*3102delinsCTTCA
NM_017849.4:c.*3098_*3102delinsCTTCA MANE Select	NP_060319.1:n.*3098_*3102delinsCTTCA