Canonical Allele Identifier: CA1272520672

Gene: TMEM127

Linked Data

• dbSNP Id: rs1684068656

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250678C>G , CM000664.2:g.96250678C>G	GRCh38
NC_000002.11:g.96916416C>G , CM000664.1:g.96916416C>G	GRCh37
NC_000002.10:g.96280143C>G	NCBI36
NG_027695.1:g.20336G>C , LRG_528:g.20336G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*3130G>C MANE Select	ENSP00000258439.3:n.*3130G>C
ENST00000258439.7:c.*3130G>C	ENSP00000258439.2:n.*3130G>C
NM_001193304.2:c.*3130G>C	NP_001180233.1:n.*3130G>C
NM_017849.3:c.*3130G>C , LRG_528t1:c.*3130G>C	NP_060319.1:n.*3130G>C
XM_017004450.1:c.*2431G>C	XP_016859939.1:n.*2431G>C
XM_017004452.1:c.*3130G>C	XP_016859941.1:n.*3130G>C
NM_001193304.3:c.*3130G>C	NP_001180233.1:n.*3130G>C
NM_017849.4:c.*3130G>C MANE Select	NP_060319.1:n.*3130G>C