Canonical Allele Identifier: CA347652298

Gene: TMEM127

Linked Data

• dbSNP Id: rs200327514
• MyVariant Identifiers: chr2:g.96919691G>C (hg19) ; chr2:g.96253953G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96253953G>C , CM000664.2:g.96253953G>C	GRCh38
NC_000002.11:g.96919691G>C , CM000664.1:g.96919691G>C	GRCh37
NC_000002.10:g.96283418G>C	NCBI36
NG_027695.1:g.17061C>G , LRG_528:g.17061C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.572C>G MANE Select	ENSP00000258439.3:p.Thr191Arg
ENST00000258439.7:c.572C>G	ENSP00000258439.2:p.Thr191Arg
ENST00000432959.1:c.572C>G	ENSP00000416660.1:p.Thr191Arg
ENST00000435268.1:c.320C>G	ENSP00000411810.1:p.Thr107Arg
NM_001193304.2:c.572C>G	NP_001180233.1:p.Thr191Arg
NM_017849.3:c.572C>G , LRG_528t1:c.572C>G	NP_060319.1:p.Thr191Arg
XM_017004450.1:c.-347C>G	XP_016859939.1:n.-347C>G
XM_017004452.1:c.320C>G	XP_016859941.1:p.Thr107Arg
NM_001193304.3:c.572C>G	NP_001180233.1:p.Thr191Arg
NM_017849.4:c.572C>G MANE Select	NP_060319.1:p.Thr191Arg