Canonical Allele Identifier: CA1272522178
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96254138A= , CM000664.2:g.96254138A= GRCh38
NC_000002.11:g.96919876A= , CM000664.1:g.96919876A= GRCh37
NC_000002.10:g.96283603A= NCBI36
NG_027695.1:g.16876T= , LRG_528:g.16876T=

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.410-23T= MANE Select ENSP00000258439.3:n.410-23T=
ENST00000258439.7:c.410-23T= ENSP00000258439.2:n.410-23T=
ENST00000432959.1:c.410-23T= ENSP00000416660.1:n.410-23T=
ENST00000435268.1:c.158-23T= ENSP00000411810.1:n.158-23T=
NM_001193304.2:c.410-23T= NP_001180233.1:n.410-23T=
NM_017849.3:c.410-23T= , LRG_528t1:c.410-23T= NP_060319.1:n.410-23T=
XM_017004450.1:c.-509-23T= XP_016859939.1:n.-509-23T=
XM_017004452.1:c.158-23T= XP_016859941.1:n.158-23T=
NM_001193304.3:c.410-23T= NP_001180233.1:n.410-23T=
NM_017849.4:c.410-23T= MANE Select NP_060319.1:n.410-23T=