Canonical Allele Identifier: CA2660175015
Gene: TMEM127 HGNC NCBI

Linked Data

gnomAD v4: 2-96251123-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251123A>T , CM000664.2:g.96251123A>T GRCh38
NC_000002.11:g.96916861A>T , CM000664.1:g.96916861A>T GRCh37
NC_000002.10:g.96280588A>T NCBI36
NG_027695.1:g.19891T>A , LRG_528:g.19891T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.*2685T>A MANE Select ENSP00000258439.3:n.*2685T>A
ENST00000258439.7:c.*2685T>A ENSP00000258439.2:n.*2685T>A
NM_001193304.2:c.*2685T>A NP_001180233.1:n.*2685T>A
NM_017849.3:c.*2685T>A , LRG_528t1:c.*2685T>A NP_060319.1:n.*2685T>A
XM_017004450.1:c.*1986T>A XP_016859939.1:n.*1986T>A
XM_017004452.1:c.*2685T>A XP_016859941.1:n.*2685T>A
NM_001193304.3:c.*2685T>A NP_001180233.1:n.*2685T>A
NM_017849.4:c.*2685T>A MANE Select NP_060319.1:n.*2685T>A
Search 100 bp 5'
Search 100 bp 3'