Canonical Allele Identifier: CA1272522559

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254973_96254977delinsACTGT , CM000664.2:g.96254973_96254977delinsACTGT	GRCh38
NC_000002.11:g.96920711_96920715delinsACTGT , CM000664.1:g.96920711_96920715delinsACTGT	GRCh37
NC_000002.10:g.96284438_96284442delinsACTGT	NCBI36
NG_027695.1:g.16037_16041delinsACAGT , LRG_528:g.16037_16041delinsACAGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.265_269delinsACAGT MANE Select	ENSP00000258439.3:p.Thr89=
ENST00000258439.7:c.265_269delinsACAGT	ENSP00000258439.2:p.Thr89=
ENST00000432959.1:c.265_269delinsACAGT	ENSP00000416660.1:p.Thr89=
ENST00000435268.1:c.13_17delinsACAGT	ENSP00000411810.1:p.Thr5=
NM_001193304.2:c.265_269delinsACAGT	NP_001180233.1:p.Thr89=
NM_017849.3:c.265_269delinsACAGT , LRG_528t1:c.265_269delinsACAGT	NP_060319.1:p.Thr89=
XM_017004450.1:c.-654_-650delinsACAGT	XP_016859939.1:n.-654_-650delinsACAGT
XM_017004452.1:c.13_17delinsACAGT	XP_016859941.1:p.Thr5=
NM_001193304.3:c.265_269delinsACAGT	NP_001180233.1:p.Thr89=
NM_017849.4:c.265_269delinsACAGT MANE Select	NP_060319.1:p.Thr89=