Canonical Allele Identifier: CA347650827

Gene: TMEM127

Linked Data

• ClinVar Variation Id: 2035952
• ClinVar RCV Id: RCV002881833
• MyVariant Identifiers: chr2:g.96919548A>T (hg19) ; chr2:g.96253810A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96253810A>T , CM000664.2:g.96253810A>T	GRCh38
NC_000002.11:g.96919548A>T , CM000664.1:g.96919548A>T	GRCh37
NC_000002.10:g.96283275A>T	NCBI36
NG_027695.1:g.17204T>A , LRG_528:g.17204T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.715T>A MANE Select	ENSP00000258439.3:p.Ter239Lys
ENST00000258439.7:c.715T>A	ENSP00000258439.2:p.Ter239Lys
ENST00000432959.1:c.715T>A	ENSP00000416660.1:p.Ter239Lys
ENST00000435268.1:c.463T>A	ENSP00000411810.1:p.Ter155Lys
NM_001193304.2:c.715T>A	NP_001180233.1:p.Ter239Lys
NM_017849.3:c.715T>A , LRG_528t1:c.715T>A	NP_060319.1:p.Ter239Lys
XM_017004450.1:c.-204T>A	XP_016859939.1:n.-204T>A
XM_017004452.1:c.463T>A	XP_016859941.1:p.Ter155Lys
NM_001193304.3:c.715T>A	NP_001180233.1:p.Ter239Lys
NM_017849.4:c.715T>A MANE Select	NP_060319.1:p.Ter239Lys