Canonical Allele Identifier: CA895768749

Gene: TMEM127

Linked Data

• dbSNP Id: rs1347089883
• MyVariant Identifiers: chr2:g.96917086_96917087del (hg19) ; chr2:g.96251348_96251349del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251351_96251352del , CM000664.2:g.96251351_96251352del	GRCh38
NC_000002.11:g.96917089_96917090del , CM000664.1:g.96917089_96917090del	GRCh37
NC_000002.10:g.96280816_96280817del	NCBI36
NG_027695.1:g.19665_19666del , LRG_528:g.19665_19666del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2459_*2460del MANE Select	ENSP00000258439.3:n.*2459_*2460del
ENST00000258439.7:c.*2459_*2460del	ENSP00000258439.2:n.*2459_*2460del
NM_001193304.2:c.*2459_*2460del	NP_001180233.1:n.*2459_*2460del
NM_017849.3:c.*2459_*2460del , LRG_528t1:c.*2459_*2460del	NP_060319.1:n.*2459_*2460del
XM_017004450.1:c.*1760_*1761del	XP_016859939.1:n.*1760_*1761del
XM_017004452.1:c.*2459_*2460del	XP_016859941.1:n.*2459_*2460del
NM_001193304.3:c.*2459_*2460del	NP_001180233.1:n.*2459_*2460del
NM_017849.4:c.*2459_*2460del MANE Select	NP_060319.1:n.*2459_*2460del