Canonical Allele Identifier: CA1272520799

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250939_96250940delinsGA , CM000664.2:g.96250939_96250940delinsGA	GRCh38
NC_000002.11:g.96916677_96916678delinsGA , CM000664.1:g.96916677_96916678delinsGA	GRCh37
NC_000002.10:g.96280404_96280405delinsGA	NCBI36
NG_027695.1:g.20074_20075delinsTC , LRG_528:g.20074_20075delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2868_*2869delinsTC MANE Select	ENSP00000258439.3:n.*2868_*2869delinsTC
ENST00000258439.7:c.*2868_*2869delinsTC	ENSP00000258439.2:n.*2868_*2869delinsTC
NM_001193304.2:c.*2868_*2869delinsTC	NP_001180233.1:n.*2868_*2869delinsTC
NM_017849.3:c.*2868_*2869delinsTC , LRG_528t1:c.*2868_*2869delinsTC	NP_060319.1:n.*2868_*2869delinsTC
XM_017004450.1:c.*2169_*2170delinsTC	XP_016859939.1:n.*2169_*2170delinsTC
XM_017004452.1:c.*2868_*2869delinsTC	XP_016859941.1:n.*2868_*2869delinsTC
NM_001193304.3:c.*2868_*2869delinsTC	NP_001180233.1:n.*2868_*2869delinsTC
NM_017849.4:c.*2868_*2869delinsTC MANE Select	NP_060319.1:n.*2868_*2869delinsTC