Canonical Allele Identifier: CA1272522105

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96253994_96253995delinsGA , CM000664.2:g.96253994_96253995delinsGA	GRCh38
NC_000002.11:g.96919732_96919733delinsGA , CM000664.1:g.96919732_96919733delinsGA	GRCh37
NC_000002.10:g.96283459_96283460delinsGA	NCBI36
NG_027695.1:g.17019_17020delinsTC , LRG_528:g.17019_17020delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.530_531delinsTC MANE Select	ENSP00000258439.3:p.Phe177=
ENST00000258439.7:c.530_531delinsTC	ENSP00000258439.2:p.Phe177=
ENST00000432959.1:c.530_531delinsTC	ENSP00000416660.1:p.Phe177=
ENST00000435268.1:c.278_279delinsTC	ENSP00000411810.1:p.Phe93=
NM_001193304.2:c.530_531delinsTC	NP_001180233.1:p.Phe177=
NM_017849.3:c.530_531delinsTC , LRG_528t1:c.530_531delinsTC	NP_060319.1:p.Phe177=
XM_017004450.1:c.-389_-388delinsTC	XP_016859939.1:n.-389_-388delinsTC
XM_017004452.1:c.278_279delinsTC	XP_016859941.1:p.Phe93=
NM_001193304.3:c.530_531delinsTC	NP_001180233.1:p.Phe177=
NM_017849.4:c.530_531delinsTC MANE Select	NP_060319.1:p.Phe177=