Canonical Allele Identifier: CA1272520681

Gene: TMEM127

Linked Data

• dbSNP Id: rs1005995212

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250703G>C , CM000664.2:g.96250703G>C	GRCh38
NC_000002.11:g.96916441G>C , CM000664.1:g.96916441G>C	GRCh37
NC_000002.10:g.96280168G>C	NCBI36
NG_027695.1:g.20311C>G , LRG_528:g.20311C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*3105C>G MANE Select	ENSP00000258439.3:n.*3105C>G
ENST00000258439.7:c.*3105C>G	ENSP00000258439.2:n.*3105C>G
NM_001193304.2:c.*3105C>G	NP_001180233.1:n.*3105C>G
NM_017849.3:c.*3105C>G , LRG_528t1:c.*3105C>G	NP_060319.1:n.*3105C>G
XM_017004450.1:c.*2406C>G	XP_016859939.1:n.*2406C>G
XM_017004452.1:c.*3105C>G	XP_016859941.1:n.*3105C>G
NM_001193304.3:c.*3105C>G	NP_001180233.1:n.*3105C>G
NM_017849.4:c.*3105C>G MANE Select	NP_060319.1:n.*3105C>G