Canonical Allele Identifier: CA1272520857

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251069_96251083delinsTTTGAAGGTTGGGCC , CM000664.2:g.96251069_96251083delinsTTTGAAGGTTGGGCC	GRCh38
NC_000002.11:g.96916807_96916821delinsTTTGAAGGTTGGGCC , CM000664.1:g.96916807_96916821delinsTTTGAAGGTTGGGCC	GRCh37
NC_000002.10:g.96280534_96280548delinsTTTGAAGGTTGGGCC	NCBI36
NG_027695.1:g.19931_19945delinsGGCCCAACCTTCAAA , LRG_528:g.19931_19945delinsGGCCCAACCTTCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2725_*2739delinsGGCCCAACCTTCAAA MANE Select	ENSP00000258439.3:n.*2725_*2739delinsGGCCCAACCTTCAAA
ENST00000258439.7:c.*2725_*2739delinsGGCCCAACCTTCAAA	ENSP00000258439.2:n.*2725_*2739delinsGGCCCAACCTTCAAA
NM_001193304.2:c.*2725_*2739delinsGGCCCAACCTTCAAA	NP_001180233.1:n.*2725_*2739delinsGGCCCAACCTTCAAA
NM_017849.3:c.*2725_*2739delinsGGCCCAACCTTCAAA , LRG_528t1:c.*2725_*2739delinsGGCCCAACCTTCAAA	NP_060319.1:n.*2725_*2739delinsGGCCCAACCTTCAAA
XM_017004450.1:c.*2026_*2040delinsGGCCCAACCTTCAAA	XP_016859939.1:n.*2026_*2040delinsGGCCCAACCTTCAAA
XM_017004452.1:c.*2725_*2739delinsGGCCCAACCTTCAAA	XP_016859941.1:n.*2725_*2739delinsGGCCCAACCTTCAAA
NM_001193304.3:c.*2725_*2739delinsGGCCCAACCTTCAAA	NP_001180233.1:n.*2725_*2739delinsGGCCCAACCTTCAAA
NM_017849.4:c.*2725_*2739delinsGGCCCAACCTTCAAA MANE Select	NP_060319.1:n.*2725_*2739delinsGGCCCAACCTTCAAA