Canonical Allele Identifier: CA1272520972
Gene: TMEM127 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251319A= , CM000664.2:g.96251319A= GRCh38
NC_000002.11:g.96917057A= , CM000664.1:g.96917057A= GRCh37
NC_000002.10:g.96280784A= NCBI36
NG_027695.1:g.19695T= , LRG_528:g.19695T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2489T= MANE Select ENSP00000258439.3:n.*2489T=
ENST00000258439.7:c.*2489T= ENSP00000258439.2:n.*2489T=
NM_001193304.2:c.*2489T= NP_001180233.1:n.*2489T=
NM_017849.3:c.*2489T= , LRG_528t1:c.*2489T= NP_060319.1:n.*2489T=
XM_017004450.1:c.*1790T= XP_016859939.1:n.*1790T=
XM_017004452.1:c.*2489T= XP_016859941.1:n.*2489T=
NM_001193304.3:c.*2489T= NP_001180233.1:n.*2489T=
NM_017849.4:c.*2489T= MANE Select NP_060319.1:n.*2489T=
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