Canonical Allele Identifier: CA1272521113
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1684090331
gnomAD v4: 2-96251638-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251638T>C , CM000664.2:g.96251638T>C GRCh38
NC_000002.11:g.96917376T>C , CM000664.1:g.96917376T>C GRCh37
NC_000002.10:g.96281103T>C NCBI36
NG_027695.1:g.19376A>G , LRG_528:g.19376A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2170A>G MANE Select ENSP00000258439.3:n.*2170A>G
ENST00000258439.7:c.*2170A>G ENSP00000258439.2:n.*2170A>G
NM_001193304.2:c.*2170A>G NP_001180233.1:n.*2170A>G
NM_017849.3:c.*2170A>G , LRG_528t1:c.*2170A>G NP_060319.1:n.*2170A>G
XM_017004450.1:c.*1471A>G XP_016859939.1:n.*1471A>G
XM_017004452.1:c.*2170A>G XP_016859941.1:n.*2170A>G
NM_001193304.3:c.*2170A>G NP_001180233.1:n.*2170A>G
NM_017849.4:c.*2170A>G MANE Select NP_060319.1:n.*2170A>G
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