Canonical Allele Identifier: CA2660177279

Gene: TMEM127

Linked Data

• gnomAD v4: 2-96254015-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254016_96254017insTT , CM000664.2:g.96254016_96254017insTT	GRCh38
NC_000002.11:g.96919754_96919755insTT , CM000664.1:g.96919754_96919755insTT	GRCh37
NC_000002.10:g.96283481_96283482insTT	NCBI36
NG_027695.1:g.16998_16999insAA , LRG_528:g.16998_16999insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.509_510insAA MANE Select	ENSP00000258439.3:p.Tyr170Ter
ENST00000258439.7:c.509_510insAA	ENSP00000258439.2:p.Tyr170Ter
ENST00000432959.1:c.509_510insAA	ENSP00000416660.1:p.Tyr170Ter
ENST00000435268.1:c.257_258insAA	ENSP00000411810.1:p.Tyr86Ter
NM_001193304.2:c.509_510insAA	NP_001180233.1:p.Tyr170Ter
NM_017849.3:c.509_510insAA , LRG_528t1:c.509_510insAA	NP_060319.1:p.Tyr170Ter
XM_017004450.1:c.-410_-409insAA	XP_016859939.1:n.-410_-409insAA
XM_017004452.1:c.257_258insAA	XP_016859941.1:p.Tyr86Ter
NM_001193304.3:c.509_510insAA	NP_001180233.1:p.Tyr170Ter
NM_017849.4:c.509_510insAA MANE Select	NP_060319.1:p.Tyr170Ter