Canonical Allele Identifier: CA703462470

Gene: TMEM121

Linked Data

• dbSNP Id: rs1347468169
• gnomAD v4: 14-105529863-T-G
• MyVariant Identifiers: chr14:g.105529863T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105529863T>G , CM000676.2:g.105529863T>G	GRCh38
NC_000014.8:g.105996200T>G , CM000676.1:g.105996200T>G	GRCh37
NC_000014.7:g.105067245T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392519.7:c.*69T>G MANE Select	ENSP00000376304.2:n.*69T>G
ENST00000392519.6:c.*69T>G	ENSP00000376304.2:n.*69T>G
ENST00000431372.1:c.*69T>G	ENSP00000407456.1:n.*69T>G
NM_025268.2:c.*69T>G	NP_079544.1:n.*69T>G
XM_005268101.2:c.*69T>G	XP_005268158.1:n.*69T>G
XM_006720261.2:c.*69T>G	XP_006720324.1:n.*69T>G
XM_011537185.1:c.*69T>G	XP_011535487.1:n.*69T>G
XM_011537186.1:c.*69T>G	XP_011535488.1:n.*69T>G
NM_001331238.1:c.*69T>G	NP_001318167.1:n.*69T>G
NM_025268.3:c.*69T>G	NP_079544.1:n.*69T>G
XM_006720261.3:c.*69T>G	XP_006720324.1:n.*69T>G
NM_025268.4:c.*69T>G MANE Select	NP_079544.1:n.*69T>G
NM_001331238.2:c.*69T>G	NP_001318167.1:n.*69T>G