Canonical Allele Identifier: CA347652929

Gene: TMEM127

Linked Data

• MyVariant Identifiers: chr2:g.96919802A>G (hg19) ; chr2:g.96254064A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254064A>G , CM000664.2:g.96254064A>G	GRCh38
NC_000002.11:g.96919802A>G , CM000664.1:g.96919802A>G	GRCh37
NC_000002.10:g.96283529A>G	NCBI36
NG_027695.1:g.16950T>C , LRG_528:g.16950T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.461T>C MANE Select	ENSP00000258439.3:p.Ile154Thr
ENST00000258439.7:c.461T>C	ENSP00000258439.2:p.Ile154Thr
ENST00000432959.1:c.461T>C	ENSP00000416660.1:p.Ile154Thr
ENST00000435268.1:c.209T>C	ENSP00000411810.1:p.Ile70Thr
NM_001193304.2:c.461T>C	NP_001180233.1:p.Ile154Thr
NM_017849.3:c.461T>C , LRG_528t1:c.461T>C	NP_060319.1:p.Ile154Thr
XM_017004450.1:c.-458T>C	XP_016859939.1:n.-458T>C
XM_017004452.1:c.209T>C	XP_016859941.1:p.Ile70Thr
NM_001193304.3:c.461T>C	NP_001180233.1:p.Ile154Thr
NM_017849.4:c.461T>C MANE Select	NP_060319.1:p.Ile154Thr