Canonical Allele Identifier: CA2161352875

Gene: TMEM121

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105529712_105529724delinsTGCCGCCGCCGCC , CM000676.2:g.105529712_105529724delinsTGCCGCCGCCGCC	GRCh38
NC_000014.8:g.105996049_105996061delinsTGCCGCCGCCGCC , CM000676.1:g.105996049_105996061delinsTGCCGCCGCCGCC	GRCh37
NC_000014.7:g.105067094_105067106delinsTGCCGCCGCCGCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392519.7:c.878_890delinsTGCCGCCGCCGCC MANE Select	ENSP00000376304.2:p.Val293=
ENST00000392519.6:c.878_890delinsTGCCGCCGCCGCC	ENSP00000376304.2:p.Val293=
ENST00000431372.1:c.878_890delinsTGCCGCCGCCGCC	ENSP00000407456.1:p.Val293=
NM_025268.2:c.878_890delinsTGCCGCCGCCGCC	NP_079544.1:p.Val293=
XM_005268101.2:c.878_890delinsTGCCGCCGCCGCC	XP_005268158.1:p.Val293=
XM_006720261.2:c.878_890delinsTGCCGCCGCCGCC	XP_006720324.1:p.Val293=
XM_011537185.1:c.878_890delinsTGCCGCCGCCGCC	XP_011535487.1:p.Val293=
XM_011537186.1:c.878_890delinsTGCCGCCGCCGCC	XP_011535488.1:p.Val293=
NM_001331238.1:c.878_890delinsTGCCGCCGCCGCC	NP_001318167.1:p.Val293=
NM_025268.3:c.878_890delinsTGCCGCCGCCGCC	NP_079544.1:p.Val293=
XM_006720261.3:c.878_890delinsTGCCGCCGCCGCC	XP_006720324.1:p.Val293=
NM_025268.4:c.878_890delinsTGCCGCCGCCGCC MANE Select	NP_079544.1:p.Val293=
NM_001331238.2:c.878_890delinsTGCCGCCGCCGCC	NP_001318167.1:p.Val293=