Canonical Allele Identifier: CA1272522639
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1684178864
gnomAD v4: 2-96255140-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96255140G>A , CM000664.2:g.96255140G>A GRCh38
NC_000002.11:g.96920878G>A , CM000664.1:g.96920878G>A GRCh37
NC_000002.10:g.96284605G>A NCBI36
NG_027695.1:g.15874C>T , LRG_528:g.15874C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.245-143C>T MANE Select ENSP00000258439.3:n.245-143C>T
ENST00000258439.7:c.245-143C>T ENSP00000258439.2:n.245-143C>T
ENST00000432959.1:c.245-143C>T ENSP00000416660.1:n.245-143C>T
ENST00000435268.1:c.-8-143C>T ENSP00000411810.1:n.-8-143C>T
NM_001193304.2:c.245-143C>T NP_001180233.1:n.245-143C>T
NM_017849.3:c.245-143C>T , LRG_528t1:c.245-143C>T NP_060319.1:n.245-143C>T
XM_017004450.1:c.-674-143C>T XP_016859939.1:n.-674-143C>T
XM_017004452.1:c.-8-143C>T XP_016859941.1:n.-8-143C>T
NM_001193304.3:c.245-143C>T NP_001180233.1:n.245-143C>T
NM_017849.4:c.245-143C>T MANE Select NP_060319.1:n.245-143C>T