Canonical Allele Identifier: CA347652690
Gene: TMEM127 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.96919760T>G (hg19) chr2:g.96254022T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96254022T>G , CM000664.2:g.96254022T>G GRCh38
NC_000002.11:g.96919760T>G , CM000664.1:g.96919760T>G GRCh37
NC_000002.10:g.96283487T>G NCBI36
NG_027695.1:g.16992A>C , LRG_528:g.16992A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.503A>C MANE Select ENSP00000258439.3:p.Gln168Pro
ENST00000258439.7:c.503A>C ENSP00000258439.2:p.Gln168Pro
ENST00000432959.1:c.503A>C ENSP00000416660.1:p.Gln168Pro
ENST00000435268.1:c.251A>C ENSP00000411810.1:p.Gln84Pro
NM_001193304.2:c.503A>C NP_001180233.1:p.Gln168Pro
NM_017849.3:c.503A>C , LRG_528t1:c.503A>C NP_060319.1:p.Gln168Pro
XM_017004450.1:c.-416A>C XP_016859939.1:n.-416A>C
XM_017004452.1:c.251A>C XP_016859941.1:p.Gln84Pro
NM_001193304.3:c.503A>C NP_001180233.1:p.Gln168Pro
NM_017849.4:c.503A>C MANE Select NP_060319.1:p.Gln168Pro
Search 100 bp 5'
Search 100 bp 3'