Canonical Allele Identifier: CA2751313996

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250918dup , CM000664.2:g.96250918dup	GRCh38
NC_000002.11:g.96916656dup , CM000664.1:g.96916656dup	GRCh37
NC_000002.10:g.96280383dup	NCBI36
NG_027695.1:g.20098dup , LRG_528:g.20098dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2892dup MANE Select	ENSP00000258439.3:n.*2892dup
ENST00000258439.7:c.*2892dup	ENSP00000258439.2:n.*2892dup
NM_001193304.2:c.*2892dup	NP_001180233.1:n.*2892dup
NM_017849.3:c.*2892dup , LRG_528t1:c.*2892dup	NP_060319.1:n.*2892dup
XM_017004450.1:c.*2193dup	XP_016859939.1:n.*2193dup
XM_017004452.1:c.*2892dup	XP_016859941.1:n.*2892dup
NM_001193304.3:c.*2892dup	NP_001180233.1:n.*2892dup
NM_017849.4:c.*2892dup MANE Select	NP_060319.1:n.*2892dup