Canonical Allele Identifier: CA427807839
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 2965133
ClinVar RCV Id: RCV003823299
dbSNP Id: rs1684145823
MyVariant Identifiers: chr2:g.96919666G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96253928G>A , CM000664.2:g.96253928G>A GRCh38
NC_000002.11:g.96919666G>A , CM000664.1:g.96919666G>A GRCh37
NC_000002.10:g.96283393G>A NCBI36
NG_027695.1:g.17086C>T , LRG_528:g.17086C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.597C>T MANE Select ENSP00000258439.3:p.Tyr199=
ENST00000258439.7:c.597C>T ENSP00000258439.2:p.Tyr199=
ENST00000432959.1:c.597C>T ENSP00000416660.1:p.Tyr199=
ENST00000435268.1:c.345C>T ENSP00000411810.1:p.Tyr115=
NM_001193304.2:c.597C>T NP_001180233.1:p.Tyr199=
NM_017849.3:c.597C>T , LRG_528t1:c.597C>T NP_060319.1:p.Tyr199=
XM_017004450.1:c.-322C>T XP_016859939.1:n.-322C>T
XM_017004452.1:c.345C>T XP_016859941.1:p.Tyr115=
NM_001193304.3:c.597C>T NP_001180233.1:p.Tyr199=
NM_017849.4:c.597C>T MANE Select NP_060319.1:p.Tyr199=