Canonical Allele Identifier: CA1272522169

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254124_96254125delinsCA , CM000664.2:g.96254124_96254125delinsCA	GRCh38
NC_000002.11:g.96919862_96919863delinsCA , CM000664.1:g.96919862_96919863delinsCA	GRCh37
NC_000002.10:g.96283589_96283590delinsCA	NCBI36
NG_027695.1:g.16889_16890delinsTG , LRG_528:g.16889_16890delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.410-10_410-9delinsTG MANE Select	ENSP00000258439.3:n.410-10_410-9delinsTG
ENST00000258439.7:c.410-10_410-9delinsTG	ENSP00000258439.2:n.410-10_410-9delinsTG
ENST00000432959.1:c.410-10_410-9delinsTG	ENSP00000416660.1:n.410-10_410-9delinsTG
ENST00000435268.1:c.158-10_158-9delinsTG	ENSP00000411810.1:n.158-10_158-9delinsTG
NM_001193304.2:c.410-10_410-9delinsTG	NP_001180233.1:n.410-10_410-9delinsTG
NM_017849.3:c.410-10_410-9delinsTG , LRG_528t1:c.410-10_410-9delinsTG	NP_060319.1:n.410-10_410-9delinsTG
XM_017004450.1:c.-509-10_-509-9delinsTG	XP_016859939.1:n.-509-10_-509-9delinsTG
XM_017004452.1:c.158-10_158-9delinsTG	XP_016859941.1:n.158-10_158-9delinsTG
NM_001193304.3:c.410-10_410-9delinsTG	NP_001180233.1:n.410-10_410-9delinsTG
NM_017849.4:c.410-10_410-9delinsTG MANE Select	NP_060319.1:n.410-10_410-9delinsTG