Canonical Allele Identifier: CA1272520791

Gene: TMEM127

Linked Data

• dbSNP Id: rs1684074514

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250930_96250932del , CM000664.2:g.96250930_96250932del	GRCh38
NC_000002.11:g.96916668_96916670del , CM000664.1:g.96916668_96916670del	GRCh37
NC_000002.10:g.96280395_96280397del	NCBI36
NG_027695.1:g.20084_20086del , LRG_528:g.20084_20086del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2878_*2880del MANE Select	ENSP00000258439.3:n.*2878_*2880del
ENST00000258439.7:c.*2878_*2880del	ENSP00000258439.2:n.*2878_*2880del
NM_001193304.2:c.*2878_*2880del	NP_001180233.1:n.*2878_*2880del
NM_017849.3:c.*2878_*2880del , LRG_528t1:c.*2878_*2880del	NP_060319.1:n.*2878_*2880del
XM_017004450.1:c.*2179_*2181del	XP_016859939.1:n.*2179_*2181del
XM_017004452.1:c.*2878_*2880del	XP_016859941.1:n.*2878_*2880del
NM_001193304.3:c.*2878_*2880del	NP_001180233.1:n.*2878_*2880del
NM_017849.4:c.*2878_*2880del MANE Select	NP_060319.1:n.*2878_*2880del