Canonical Allele Identifier: CA2660175009
Gene: TMEM127 HGNC NCBI

Linked Data

gnomAD v4: 2-96251114-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251114G>C , CM000664.2:g.96251114G>C GRCh38
NC_000002.11:g.96916852G>C , CM000664.1:g.96916852G>C GRCh37
NC_000002.10:g.96280579G>C NCBI36
NG_027695.1:g.19900C>G , LRG_528:g.19900C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2694C>G MANE Select ENSP00000258439.3:n.*2694C>G
ENST00000258439.7:c.*2694C>G ENSP00000258439.2:n.*2694C>G
NM_001193304.2:c.*2694C>G NP_001180233.1:n.*2694C>G
NM_017849.3:c.*2694C>G , LRG_528t1:c.*2694C>G NP_060319.1:n.*2694C>G
XM_017004450.1:c.*1995C>G XP_016859939.1:n.*1995C>G
XM_017004452.1:c.*2694C>G XP_016859941.1:n.*2694C>G
NM_001193304.3:c.*2694C>G NP_001180233.1:n.*2694C>G
NM_017849.4:c.*2694C>G MANE Select NP_060319.1:n.*2694C>G
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