Canonical Allele Identifier: CA488509511

Gene: TMEM121

Linked Data

• dbSNP Id: rs895624821
• gnomAD v3: 14-105529740-C-G
• gnomAD v4: 14-105529740-C-G
• MyVariant Identifiers: chr14:g.105996077C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105529740C>G , CM000676.2:g.105529740C>G	GRCh38
NC_000014.8:g.105996077C>G , CM000676.1:g.105996077C>G	GRCh37
NC_000014.7:g.105067122C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392519.7:c.906C>G MANE Select	ENSP00000376304.2:p.Gly302=
ENST00000392519.6:c.906C>G	ENSP00000376304.2:p.Gly302=
ENST00000431372.1:c.906C>G	ENSP00000407456.1:p.Gly302=
NM_025268.2:c.906C>G	NP_079544.1:p.Gly302=
XM_005268101.2:c.906C>G	XP_005268158.1:p.Gly302=
XM_006720261.2:c.906C>G	XP_006720324.1:p.Gly302=
XM_011537185.1:c.906C>G	XP_011535487.1:p.Gly302=
XM_011537186.1:c.906C>G	XP_011535488.1:p.Gly302=
NM_001331238.1:c.906C>G	NP_001318167.1:p.Gly302=
NM_025268.3:c.906C>G	NP_079544.1:p.Gly302=
XM_006720261.3:c.906C>G	XP_006720324.1:p.Gly302=
NM_025268.4:c.906C>G MANE Select	NP_079544.1:p.Gly302=
NM_001331238.2:c.906C>G	NP_001318167.1:p.Gly302=