Canonical Allele Identifier: CA1272522174
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96254132C= , CM000664.2:g.96254132C= GRCh38
NC_000002.11:g.96919870C= , CM000664.1:g.96919870C= GRCh37
NC_000002.10:g.96283597C= NCBI36
NG_027695.1:g.16882G= , LRG_528:g.16882G=

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.410-17G= MANE Select ENSP00000258439.3:n.410-17G=
ENST00000258439.7:c.410-17G= ENSP00000258439.2:n.410-17G=
ENST00000432959.1:c.410-17G= ENSP00000416660.1:n.410-17G=
ENST00000435268.1:c.158-17G= ENSP00000411810.1:n.158-17G=
NM_001193304.2:c.410-17G= NP_001180233.1:n.410-17G=
NM_017849.3:c.410-17G= , LRG_528t1:c.410-17G= NP_060319.1:n.410-17G=
XM_017004450.1:c.-509-17G= XP_016859939.1:n.-509-17G=
XM_017004452.1:c.158-17G= XP_016859941.1:n.158-17G=
NM_001193304.3:c.410-17G= NP_001180233.1:n.410-17G=
NM_017849.4:c.410-17G= MANE Select NP_060319.1:n.410-17G=