Canonical Allele Identifier: CA7391508

Gene: TMEM121

Linked Data

• dbSNP Id: rs10569304
• ExAC: 14:105996049 TGCCGCCGCCGCC / T
• gnomAD v2: 14-105996049-TGCCGCCGCCGCC-T
• gnomAD v3: 14-105529712-TGCCGCCGCCGCC-T
• gnomAD v4: 14-105529712-TGCCGCCGCCGCC-T
• MyVariant Identifiers: chr14:g.105996050_105996061del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105529721_105529732del , CM000676.2:g.105529721_105529732del	GRCh38
NC_000014.8:g.105996058_105996069del , CM000676.1:g.105996058_105996069del	GRCh37
NC_000014.7:g.105067103_105067114del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392519.7:c.887_898del MANE Select	ENSP00000376304.2:p.Pro296_Pro299del
ENST00000392519.6:c.887_898del	ENSP00000376304.2:p.Pro296_Pro299del
ENST00000431372.1:c.887_898del	ENSP00000407456.1:p.Pro296_Pro299del
NM_025268.2:c.887_898del	NP_079544.1:p.Pro296_Pro299del
XM_005268101.2:c.887_898del	XP_005268158.1:p.Pro296_Pro299del
XM_006720261.2:c.887_898del	XP_006720324.1:p.Pro296_Pro299del
XM_011537185.1:c.887_898del	XP_011535487.1:p.Pro296_Pro299del
XM_011537186.1:c.887_898del	XP_011535488.1:p.Pro296_Pro299del
NM_001331238.1:c.887_898del	NP_001318167.1:p.Pro296_Pro299del
NM_025268.3:c.887_898del	NP_079544.1:p.Pro296_Pro299del
XM_006720261.3:c.887_898del	XP_006720324.1:p.Pro296_Pro299del
NM_025268.4:c.887_898del MANE Select	NP_079544.1:p.Pro296_Pro299del
NM_001331238.2:c.887_898del	NP_001318167.1:p.Pro296_Pro299del