Canonical Allele Identifier: CA2660177580

Gene: TMEM127

Linked Data

• gnomAD v4: 2-96254184-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254184C>A , CM000664.2:g.96254184C>A	GRCh38
NC_000002.11:g.96919922C>A , CM000664.1:g.96919922C>A	GRCh37
NC_000002.10:g.96283649C>A	NCBI36
NG_027695.1:g.16830G>T , LRG_528:g.16830G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.410-69G>T MANE Select	ENSP00000258439.3:n.410-69G>T
ENST00000258439.7:c.410-69G>T	ENSP00000258439.2:n.410-69G>T
ENST00000432959.1:c.410-69G>T	ENSP00000416660.1:n.410-69G>T
ENST00000435268.1:c.158-69G>T	ENSP00000411810.1:n.158-69G>T
NM_001193304.2:c.410-69G>T	NP_001180233.1:n.410-69G>T
NM_017849.3:c.410-69G>T , LRG_528t1:c.410-69G>T	NP_060319.1:n.410-69G>T
XM_017004450.1:c.-509-69G>T	XP_016859939.1:n.-509-69G>T
XM_017004452.1:c.158-69G>T	XP_016859941.1:n.158-69G>T
NM_001193304.3:c.410-69G>T	NP_001180233.1:n.410-69G>T
NM_017849.4:c.410-69G>T MANE Select	NP_060319.1:n.410-69G>T