Canonical Allele Identifier: CA1272522165
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96254119G= , CM000664.2:g.96254119G= GRCh38
NC_000002.11:g.96919857G= , CM000664.1:g.96919857G= GRCh37
NC_000002.10:g.96283584G= NCBI36
NG_027695.1:g.16895C= , LRG_528:g.16895C=

Transcript Alleles

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