Canonical Allele Identifier: CA1272521479
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1684113283
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96252448G>C , CM000664.2:g.96252448G>C GRCh38
NC_000002.11:g.96918186G>C , CM000664.1:g.96918186G>C GRCh37
NC_000002.10:g.96281913G>C NCBI36
NG_027695.1:g.18566C>G , LRG_528:g.18566C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.*1360C>G MANE Select ENSP00000258439.3:n.*1360C>G
ENST00000258439.7:c.*1360C>G ENSP00000258439.2:n.*1360C>G
ENST00000432959.1:c.*1360C>G ENSP00000416660.1:n.*1360C>G
NM_001193304.2:c.*1360C>G NP_001180233.1:n.*1360C>G
NM_017849.3:c.*1360C>G , LRG_528t1:c.*1360C>G NP_060319.1:n.*1360C>G
XM_017004450.1:c.*661C>G XP_016859939.1:n.*661C>G
XM_017004452.1:c.*1360C>G XP_016859941.1:n.*1360C>G
NM_001193304.3:c.*1360C>G NP_001180233.1:n.*1360C>G
NM_017849.4:c.*1360C>G MANE Select NP_060319.1:n.*1360C>G
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