Canonical Allele Identifier: CA391203828

Gene: TMEM121

Linked Data

• MyVariant Identifiers: chr14:g.105996123G>C (hg19) ; chr14:g.105529786G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105529786G>C , CM000676.2:g.105529786G>C	GRCh38
NC_000014.8:g.105996123G>C , CM000676.1:g.105996123G>C	GRCh37
NC_000014.7:g.105067168G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392519.7:c.952G>C MANE Select	ENSP00000376304.2:p.Asp318His
ENST00000392519.6:c.952G>C	ENSP00000376304.2:p.Asp318His
ENST00000431372.1:c.952G>C	ENSP00000407456.1:p.Asp318His
NM_025268.2:c.952G>C	NP_079544.1:p.Asp318His
XM_005268101.2:c.952G>C	XP_005268158.1:p.Asp318His
XM_006720261.2:c.952G>C	XP_006720324.1:p.Asp318His
XM_011537185.1:c.952G>C	XP_011535487.1:p.Asp318His
XM_011537186.1:c.952G>C	XP_011535488.1:p.Asp318His
NM_001331238.1:c.952G>C	NP_001318167.1:p.Asp318His
NM_025268.3:c.952G>C	NP_079544.1:p.Asp318His
XM_006720261.3:c.952G>C	XP_006720324.1:p.Asp318His
NM_025268.4:c.952G>C MANE Select	NP_079544.1:p.Asp318His
NM_001331238.2:c.952G>C	NP_001318167.1:p.Asp318His