Canonical Allele Identifier: CA2161352952

Gene: TMEM121

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105529832A= , CM000676.2:g.105529832A=	GRCh38
NC_000014.8:g.105996169A= , CM000676.1:g.105996169A=	GRCh37
NC_000014.7:g.105067214A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392519.7:c.*38A= MANE Select	ENSP00000376304.2:n.*38A=
ENST00000392519.6:c.*38A=	ENSP00000376304.2:n.*38A=
ENST00000431372.1:c.*38A=	ENSP00000407456.1:n.*38A=
NM_025268.2:c.*38A=	NP_079544.1:n.*38A=
XM_005268101.2:c.*38A=	XP_005268158.1:n.*38A=
XM_006720261.2:c.*38A=	XP_006720324.1:n.*38A=
XM_011537185.1:c.*38A=	XP_011535487.1:n.*38A=
XM_011537186.1:c.*38A=	XP_011535488.1:n.*38A=
NM_001331238.1:c.*38A=	NP_001318167.1:n.*38A=
NM_025268.3:c.*38A=	NP_079544.1:n.*38A=
XM_006720261.3:c.*38A=	XP_006720324.1:n.*38A=
NM_025268.4:c.*38A= MANE Select	NP_079544.1:n.*38A=
NM_001331238.2:c.*38A=	NP_001318167.1:n.*38A=