Canonical Allele Identifier: CA1272520626
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96250580_96250581delinsGA , CM000664.2:g.96250580_96250581delinsGA GRCh38
NC_000002.11:g.96916318_96916319delinsGA , CM000664.1:g.96916318_96916319delinsGA GRCh37
NC_000002.10:g.96280045_96280046delinsGA NCBI36
NG_027695.1:g.20433_20434delinsTC , LRG_528:g.20433_20434delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.*3227_*3228delinsTC MANE Select ENSP00000258439.3:n.*3227_*3228delinsTC
ENST00000258439.7:c.*3227_*3228delinsTC ENSP00000258439.2:n.*3227_*3228delinsTC
NM_001193304.2:c.*3227_*3228delinsTC NP_001180233.1:n.*3227_*3228delinsTC
NM_017849.3:c.*3227_*3228delinsTC , LRG_528t1:c.*3227_*3228delinsTC NP_060319.1:n.*3227_*3228delinsTC
XM_017004450.1:c.*2528_*2529delinsTC XP_016859939.1:n.*2528_*2529delinsTC
XM_017004452.1:c.*3227_*3228delinsTC XP_016859941.1:n.*3227_*3228delinsTC
NM_001193304.3:c.*3227_*3228delinsTC NP_001180233.1:n.*3227_*3228delinsTC
NM_017849.4:c.*3227_*3228delinsTC MANE Select NP_060319.1:n.*3227_*3228delinsTC