Canonical Allele Identifier: CA1272520796

Gene: TMEM127

Linked Data

• dbSNP Id: rs1684074836
• gnomAD v4: 2-96250936-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250939dup , CM000664.2:g.96250939dup	GRCh38
NC_000002.11:g.96916677dup , CM000664.1:g.96916677dup	GRCh37
NC_000002.10:g.96280404dup	NCBI36
NG_027695.1:g.20077dup , LRG_528:g.20077dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2871dup MANE Select	ENSP00000258439.3:n.*2871dup
ENST00000258439.7:c.*2871dup	ENSP00000258439.2:n.*2871dup
NM_001193304.2:c.*2871dup	NP_001180233.1:n.*2871dup
NM_017849.3:c.*2871dup , LRG_528t1:c.*2871dup	NP_060319.1:n.*2871dup
XM_017004450.1:c.*2172dup	XP_016859939.1:n.*2172dup
XM_017004452.1:c.*2871dup	XP_016859941.1:n.*2871dup
NM_001193304.3:c.*2871dup	NP_001180233.1:n.*2871dup
NM_017849.4:c.*2871dup MANE Select	NP_060319.1:n.*2871dup