Canonical Allele Identifier: CA1272520638

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250618C= , CM000664.2:g.96250618C=	GRCh38
NC_000002.11:g.96916356C= , CM000664.1:g.96916356C=	GRCh37
NC_000002.10:g.96280083C=	NCBI36
NG_027695.1:g.20396G= , LRG_528:g.20396G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*3190G= MANE Select	ENSP00000258439.3:n.*3190G=
ENST00000258439.7:c.*3190G=	ENSP00000258439.2:n.*3190G=
NM_001193304.2:c.*3190G=	NP_001180233.1:n.*3190G=
NM_017849.3:c.*3190G= , LRG_528t1:c.*3190G=	NP_060319.1:n.*3190G=
XM_017004450.1:c.*2491G=	XP_016859939.1:n.*2491G=
XM_017004452.1:c.*3190G=	XP_016859941.1:n.*3190G=
NM_001193304.3:c.*3190G=	NP_001180233.1:n.*3190G=
NM_017849.4:c.*3190G= MANE Select	NP_060319.1:n.*3190G=