Canonical Allele Identifier: CA1272520770
Gene: TMEM127 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96250874G= , CM000664.2:g.96250874G= GRCh38
NC_000002.11:g.96916612G= , CM000664.1:g.96916612G= GRCh37
NC_000002.10:g.96280339G= NCBI36
NG_027695.1:g.20140C= , LRG_528:g.20140C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2934C= MANE Select ENSP00000258439.3:n.*2934C=
ENST00000258439.7:c.*2934C= ENSP00000258439.2:n.*2934C=
NM_001193304.2:c.*2934C= NP_001180233.1:n.*2934C=
NM_017849.3:c.*2934C= , LRG_528t1:c.*2934C= NP_060319.1:n.*2934C=
XM_017004450.1:c.*2235C= XP_016859939.1:n.*2235C=
XM_017004452.1:c.*2934C= XP_016859941.1:n.*2934C=
NM_001193304.3:c.*2934C= NP_001180233.1:n.*2934C=
NM_017849.4:c.*2934C= MANE Select NP_060319.1:n.*2934C=
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