Canonical Allele Identifier: CA1272520685

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250709_96250710delinsAG , CM000664.2:g.96250709_96250710delinsAG	GRCh38
NC_000002.11:g.96916447_96916448delinsAG , CM000664.1:g.96916447_96916448delinsAG	GRCh37
NC_000002.10:g.96280174_96280175delinsAG	NCBI36
NG_027695.1:g.20304_20305delinsCT , LRG_528:g.20304_20305delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*3098_*3099delinsCT MANE Select	ENSP00000258439.3:n.*3098_*3099delinsCT
ENST00000258439.7:c.*3098_*3099delinsCT	ENSP00000258439.2:n.*3098_*3099delinsCT
NM_001193304.2:c.*3098_*3099delinsCT	NP_001180233.1:n.*3098_*3099delinsCT
NM_017849.3:c.*3098_*3099delinsCT , LRG_528t1:c.*3098_*3099delinsCT	NP_060319.1:n.*3098_*3099delinsCT
XM_017004450.1:c.*2399_*2400delinsCT	XP_016859939.1:n.*2399_*2400delinsCT
XM_017004452.1:c.*3098_*3099delinsCT	XP_016859941.1:n.*3098_*3099delinsCT
NM_001193304.3:c.*3098_*3099delinsCT	NP_001180233.1:n.*3098_*3099delinsCT
NM_017849.4:c.*3098_*3099delinsCT MANE Select	NP_060319.1:n.*3098_*3099delinsCT