Canonical Allele Identifier: CA1272520858

Gene: TMEM127

Linked Data

• dbSNP Id: rs1684077566

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251073_96251086del , CM000664.2:g.96251073_96251086del	GRCh38
NC_000002.11:g.96916811_96916824del , CM000664.1:g.96916811_96916824del	GRCh37
NC_000002.10:g.96280538_96280551del	NCBI36
NG_027695.1:g.19931_19944del , LRG_528:g.19931_19944del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2725_*2738del MANE Select	ENSP00000258439.3:n.*2725_*2738del
ENST00000258439.7:c.*2725_*2738del	ENSP00000258439.2:n.*2725_*2738del
NM_001193304.2:c.*2725_*2738del	NP_001180233.1:n.*2725_*2738del
NM_017849.3:c.*2725_*2738del , LRG_528t1:c.*2725_*2738del	NP_060319.1:n.*2725_*2738del
XM_017004450.1:c.*2026_*2039del	XP_016859939.1:n.*2026_*2039del
XM_017004452.1:c.*2725_*2738del	XP_016859941.1:n.*2725_*2738del
NM_001193304.3:c.*2725_*2738del	NP_001180233.1:n.*2725_*2738del
NM_017849.4:c.*2725_*2738del MANE Select	NP_060319.1:n.*2725_*2738del