Canonical Allele Identifier: CA1033957962

Gene: TMEM127

Linked Data

• dbSNP Id: rs1684156003
• gnomAD v3: 2-96254253-G-C
• gnomAD v4: 2-96254253-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254253G>C , CM000664.2:g.96254253G>C	GRCh38
NC_000002.11:g.96919991G>C , CM000664.1:g.96919991G>C	GRCh37
NC_000002.10:g.96283718G>C	NCBI36
NG_027695.1:g.16761C>G , LRG_528:g.16761C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.410-138C>G MANE Select	ENSP00000258439.3:n.410-138C>G
ENST00000258439.7:c.410-138C>G	ENSP00000258439.2:n.410-138C>G
ENST00000432959.1:c.410-138C>G	ENSP00000416660.1:n.410-138C>G
ENST00000435268.1:c.158-138C>G	ENSP00000411810.1:n.158-138C>G
NM_001193304.2:c.410-138C>G	NP_001180233.1:n.410-138C>G
NM_017849.3:c.410-138C>G , LRG_528t1:c.410-138C>G	NP_060319.1:n.410-138C>G
XM_017004450.1:c.-509-138C>G	XP_016859939.1:n.-509-138C>G
XM_017004452.1:c.158-138C>G	XP_016859941.1:n.158-138C>G
NM_001193304.3:c.410-138C>G	NP_001180233.1:n.410-138C>G
NM_017849.4:c.410-138C>G MANE Select	NP_060319.1:n.410-138C>G