Canonical Allele Identifier: CA427807879

Gene: TMEM127

Linked Data

• dbSNP Id: rs147816248
• MyVariant Identifiers: chr2:g.96919690C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96253952C>G , CM000664.2:g.96253952C>G	GRCh38
NC_000002.11:g.96919690C>G , CM000664.1:g.96919690C>G	GRCh37
NC_000002.10:g.96283417C>G	NCBI36
NG_027695.1:g.17062G>C , LRG_528:g.17062G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.573G>C MANE Select	ENSP00000258439.3:p.Thr191=
ENST00000258439.7:c.573G>C	ENSP00000258439.2:p.Thr191=
ENST00000432959.1:c.573G>C	ENSP00000416660.1:p.Thr191=
ENST00000435268.1:c.321G>C	ENSP00000411810.1:p.Thr107=
NM_001193304.2:c.573G>C	NP_001180233.1:p.Thr191=
NM_017849.3:c.573G>C , LRG_528t1:c.573G>C	NP_060319.1:p.Thr191=
XM_017004450.1:c.-346G>C	XP_016859939.1:n.-346G>C
XM_017004452.1:c.321G>C	XP_016859941.1:p.Thr107=
NM_001193304.3:c.573G>C	NP_001180233.1:p.Thr191=
NM_017849.4:c.573G>C MANE Select	NP_060319.1:p.Thr191=