Canonical Allele Identifier: CA1272522192

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254172T= , CM000664.2:g.96254172T=	GRCh38
NC_000002.11:g.96919910T= , CM000664.1:g.96919910T=	GRCh37
NC_000002.10:g.96283637T=	NCBI36
NG_027695.1:g.16842A= , LRG_528:g.16842A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.410-57A= MANE Select	ENSP00000258439.3:n.410-57A=
ENST00000258439.7:c.410-57A=	ENSP00000258439.2:n.410-57A=
ENST00000432959.1:c.410-57A=	ENSP00000416660.1:n.410-57A=
ENST00000435268.1:c.158-57A=	ENSP00000411810.1:n.158-57A=
NM_001193304.2:c.410-57A=	NP_001180233.1:n.410-57A=
NM_017849.3:c.410-57A= , LRG_528t1:c.410-57A=	NP_060319.1:n.410-57A=
XM_017004450.1:c.-509-57A=	XP_016859939.1:n.-509-57A=
XM_017004452.1:c.158-57A=	XP_016859941.1:n.158-57A=
NM_001193304.3:c.410-57A=	NP_001180233.1:n.410-57A=
NM_017849.4:c.410-57A= MANE Select	NP_060319.1:n.410-57A=