Canonical Allele Identifier: CA1272520771
Gene: TMEM127 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96250880T= , CM000664.2:g.96250880T= GRCh38
NC_000002.11:g.96916618T= , CM000664.1:g.96916618T= GRCh37
NC_000002.10:g.96280345T= NCBI36
NG_027695.1:g.20134A= , LRG_528:g.20134A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2928A= MANE Select ENSP00000258439.3:n.*2928A=
ENST00000258439.7:c.*2928A= ENSP00000258439.2:n.*2928A=
NM_001193304.2:c.*2928A= NP_001180233.1:n.*2928A=
NM_017849.3:c.*2928A= , LRG_528t1:c.*2928A= NP_060319.1:n.*2928A=
XM_017004450.1:c.*2229A= XP_016859939.1:n.*2229A=
XM_017004452.1:c.*2928A= XP_016859941.1:n.*2928A=
NM_001193304.3:c.*2928A= NP_001180233.1:n.*2928A=
NM_017849.4:c.*2928A= MANE Select NP_060319.1:n.*2928A=
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