Canonical Allele Identifier: CA427495547

Gene: TMEM127

Linked Data

• ClinVar Variation Id: 1652290
• ClinVar RCV Id: RCV002154463 ; RCV002434577
• dbSNP Id: rs1684173194
• MyVariant Identifiers: chr2:g.96920686G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254948G>A , CM000664.2:g.96254948G>A	GRCh38
NC_000002.11:g.96920686G>A , CM000664.1:g.96920686G>A	GRCh37
NC_000002.10:g.96284413G>A	NCBI36
NG_027695.1:g.16066C>T , LRG_528:g.16066C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.294C>T MANE Select	ENSP00000258439.3:p.Ala98=
ENST00000258439.7:c.294C>T	ENSP00000258439.2:p.Ala98=
ENST00000432959.1:c.294C>T	ENSP00000416660.1:p.Ala98=
ENST00000435268.1:c.42C>T	ENSP00000411810.1:p.Ala14=
NM_001193304.2:c.294C>T	NP_001180233.1:p.Ala98=
NM_017849.3:c.294C>T , LRG_528t1:c.294C>T	NP_060319.1:p.Ala98=
XM_017004450.1:c.-625C>T	XP_016859939.1:n.-625C>T
XM_017004452.1:c.42C>T	XP_016859941.1:p.Ala14=
NM_001193304.3:c.294C>T	NP_001180233.1:p.Ala98=
NM_017849.4:c.294C>T MANE Select	NP_060319.1:p.Ala98=