Canonical Allele Identifier: CA347653397

Gene: TMEM127

Linked Data

• ClinVar Variation Id: 1399252
• ClinVar RCV Id: RCV001893753
• dbSNP Id: rs2104287263
• MyVariant Identifiers: chr2:g.96920639T>A (hg19) ; chr2:g.96254901T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254901T>A , CM000664.2:g.96254901T>A	GRCh38
NC_000002.11:g.96920639T>A , CM000664.1:g.96920639T>A	GRCh37
NC_000002.10:g.96284366T>A	NCBI36
NG_027695.1:g.16113A>T , LRG_528:g.16113A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.341A>T MANE Select	ENSP00000258439.3:p.Asp114Val
ENST00000258439.7:c.341A>T	ENSP00000258439.2:p.Asp114Val
ENST00000432959.1:c.341A>T	ENSP00000416660.1:p.Asp114Val
ENST00000435268.1:c.89A>T	ENSP00000411810.1:p.Asp30Val
NM_001193304.2:c.341A>T	NP_001180233.1:p.Asp114Val
NM_017849.3:c.341A>T , LRG_528t1:c.341A>T	NP_060319.1:p.Asp114Val
XM_017004450.1:c.-578A>T	XP_016859939.1:n.-578A>T
XM_017004452.1:c.89A>T	XP_016859941.1:p.Asp30Val
NM_001193304.3:c.341A>T	NP_001180233.1:p.Asp114Val
NM_017849.4:c.341A>T MANE Select	NP_060319.1:p.Asp114Val