Canonical Allele Identifier: CA1272520678

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250688G= , CM000664.2:g.96250688G=	GRCh38
NC_000002.11:g.96916426G= , CM000664.1:g.96916426G=	GRCh37
NC_000002.10:g.96280153G=	NCBI36
NG_027695.1:g.20326C= , LRG_528:g.20326C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*3120C= MANE Select	ENSP00000258439.3:n.*3120C=
ENST00000258439.7:c.*3120C=	ENSP00000258439.2:n.*3120C=
NM_001193304.2:c.*3120C=	NP_001180233.1:n.*3120C=
NM_017849.3:c.*3120C= , LRG_528t1:c.*3120C=	NP_060319.1:n.*3120C=
XM_017004450.1:c.*2421C=	XP_016859939.1:n.*2421C=
XM_017004452.1:c.*3120C=	XP_016859941.1:n.*3120C=
NM_001193304.3:c.*3120C=	NP_001180233.1:n.*3120C=
NM_017849.4:c.*3120C= MANE Select	NP_060319.1:n.*3120C=