Canonical Allele Identifier: CA2660177597

Gene: TMEM127

Linked Data

• gnomAD v4: 2-96254199-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254199T>G , CM000664.2:g.96254199T>G	GRCh38
NC_000002.11:g.96919937T>G , CM000664.1:g.96919937T>G	GRCh37
NC_000002.10:g.96283664T>G	NCBI36
NG_027695.1:g.16815A>C , LRG_528:g.16815A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.410-84A>C MANE Select	ENSP00000258439.3:n.410-84A>C
ENST00000258439.7:c.410-84A>C	ENSP00000258439.2:n.410-84A>C
ENST00000432959.1:c.410-84A>C	ENSP00000416660.1:n.410-84A>C
ENST00000435268.1:c.158-84A>C	ENSP00000411810.1:n.158-84A>C
NM_001193304.2:c.410-84A>C	NP_001180233.1:n.410-84A>C
NM_017849.3:c.410-84A>C , LRG_528t1:c.410-84A>C	NP_060319.1:n.410-84A>C
XM_017004450.1:c.-509-84A>C	XP_016859939.1:n.-509-84A>C
XM_017004452.1:c.158-84A>C	XP_016859941.1:n.158-84A>C
NM_001193304.3:c.410-84A>C	NP_001180233.1:n.410-84A>C
NM_017849.4:c.410-84A>C MANE Select	NP_060319.1:n.410-84A>C