Canonical Allele Identifier: CA347652238

Gene: TMEM127

Linked Data

• dbSNP Id: rs2104283872
• MyVariant Identifiers: chr2:g.96919685G>C (hg19) ; chr2:g.96253947G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96253947G>C , CM000664.2:g.96253947G>C	GRCh38
NC_000002.11:g.96919685G>C , CM000664.1:g.96919685G>C	GRCh37
NC_000002.10:g.96283412G>C	NCBI36
NG_027695.1:g.17067C>G , LRG_528:g.17067C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.578C>G MANE Select	ENSP00000258439.3:p.Ala193Gly
ENST00000258439.7:c.578C>G	ENSP00000258439.2:p.Ala193Gly
ENST00000432959.1:c.578C>G	ENSP00000416660.1:p.Ala193Gly
ENST00000435268.1:c.326C>G	ENSP00000411810.1:p.Ala109Gly
NM_001193304.2:c.578C>G	NP_001180233.1:p.Ala193Gly
NM_017849.3:c.578C>G , LRG_528t1:c.578C>G	NP_060319.1:p.Ala193Gly
XM_017004450.1:c.-341C>G	XP_016859939.1:n.-341C>G
XM_017004452.1:c.326C>G	XP_016859941.1:p.Ala109Gly
NM_001193304.3:c.578C>G	NP_001180233.1:p.Ala193Gly
NM_017849.4:c.578C>G MANE Select	NP_060319.1:p.Ala193Gly