Canonical Allele Identifier: CA347652790

Gene: TMEM127

Linked Data

• MyVariant Identifiers: chr2:g.96919778T>G (hg19) ; chr2:g.96254040T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254040T>G , CM000664.2:g.96254040T>G	GRCh38
NC_000002.11:g.96919778T>G , CM000664.1:g.96919778T>G	GRCh37
NC_000002.10:g.96283505T>G	NCBI36
NG_027695.1:g.16974A>C , LRG_528:g.16974A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.485A>C MANE Select	ENSP00000258439.3:p.Lys162Thr
ENST00000258439.7:c.485A>C	ENSP00000258439.2:p.Lys162Thr
ENST00000432959.1:c.485A>C	ENSP00000416660.1:p.Lys162Thr
ENST00000435268.1:c.233A>C	ENSP00000411810.1:p.Lys78Thr
NM_001193304.2:c.485A>C	NP_001180233.1:p.Lys162Thr
NM_017849.3:c.485A>C , LRG_528t1:c.485A>C	NP_060319.1:p.Lys162Thr
XM_017004450.1:c.-434A>C	XP_016859939.1:n.-434A>C
XM_017004452.1:c.233A>C	XP_016859941.1:p.Lys78Thr
NM_001193304.3:c.485A>C	NP_001180233.1:p.Lys162Thr
NM_017849.4:c.485A>C MANE Select	NP_060319.1:p.Lys162Thr