Canonical Allele Identifier: CA1272521058

Gene: TMEM127

Linked Data

• dbSNP Id: rs1684087018
• gnomAD v4: 2-96251503-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251504dup , CM000664.2:g.96251504dup	GRCh38
NC_000002.11:g.96917242dup , CM000664.1:g.96917242dup	GRCh37
NC_000002.10:g.96280969dup	NCBI36
NG_027695.1:g.19510dup , LRG_528:g.19510dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*2304dup MANE Select	ENSP00000258439.3:n.*2304dup
ENST00000258439.7:c.*2304dup	ENSP00000258439.2:n.*2304dup
NM_001193304.2:c.*2304dup	NP_001180233.1:n.*2304dup
NM_017849.3:c.*2304dup , LRG_528t1:c.*2304dup	NP_060319.1:n.*2304dup
XM_017004450.1:c.*1605dup	XP_016859939.1:n.*1605dup
XM_017004452.1:c.*2304dup	XP_016859941.1:n.*2304dup
NM_001193304.3:c.*2304dup	NP_001180233.1:n.*2304dup
NM_017849.4:c.*2304dup MANE Select	NP_060319.1:n.*2304dup