Canonical Allele Identifier: CA1272520786
Gene: TMEM127 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96250907C= , CM000664.2:g.96250907C= GRCh38
NC_000002.11:g.96916645C= , CM000664.1:g.96916645C= GRCh37
NC_000002.10:g.96280372C= NCBI36
NG_027695.1:g.20107G= , LRG_528:g.20107G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2901G= MANE Select ENSP00000258439.3:n.*2901G=
ENST00000258439.7:c.*2901G= ENSP00000258439.2:n.*2901G=
NM_001193304.2:c.*2901G= NP_001180233.1:n.*2901G=
NM_017849.3:c.*2901G= , LRG_528t1:c.*2901G= NP_060319.1:n.*2901G=
XM_017004450.1:c.*2202G= XP_016859939.1:n.*2202G=
XM_017004452.1:c.*2901G= XP_016859941.1:n.*2901G=
NM_001193304.3:c.*2901G= NP_001180233.1:n.*2901G=
NM_017849.4:c.*2901G= MANE Select NP_060319.1:n.*2901G=
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