Canonical Allele Identifier: CA2575647090

Gene: TMEM121

Linked Data

• gnomAD v3: 14-105529712-T-TGCCGCC
• gnomAD v4: 14-105529712-T-TGCCGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105529727_105529732dup , CM000676.2:g.105529727_105529732dup	GRCh38
NC_000014.8:g.105996064_105996069dup , CM000676.1:g.105996064_105996069dup	GRCh37
NC_000014.7:g.105067109_105067114dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392519.7:c.893_898dup MANE Select	ENSP00000376304.2:p.Pro299_Leu300insProPro
ENST00000392519.6:c.893_898dup	ENSP00000376304.2:p.Pro299_Leu300insProPro
ENST00000431372.1:c.893_898dup	ENSP00000407456.1:p.Pro299_Leu300insProPro
NM_025268.2:c.893_898dup	NP_079544.1:p.Pro299_Leu300insProPro
XM_005268101.2:c.893_898dup	XP_005268158.1:p.Pro299_Leu300insProPro
XM_006720261.2:c.893_898dup	XP_006720324.1:p.Pro299_Leu300insProPro
XM_011537185.1:c.893_898dup	XP_011535487.1:p.Pro299_Leu300insProPro
XM_011537186.1:c.893_898dup	XP_011535488.1:p.Pro299_Leu300insProPro
NM_001331238.1:c.893_898dup	NP_001318167.1:p.Pro299_Leu300insProPro
NM_025268.3:c.893_898dup	NP_079544.1:p.Pro299_Leu300insProPro
XM_006720261.3:c.893_898dup	XP_006720324.1:p.Pro299_Leu300insProPro
NM_025268.4:c.893_898dup MANE Select	NP_079544.1:p.Pro299_Leu300insProPro
NM_001331238.2:c.893_898dup	NP_001318167.1:p.Pro299_Leu300insProPro