Canonical Allele Identifier: CA393979143

Gene: TM2D3

Linked Data

• MyVariant Identifiers: chr15:g.102186988A>T (hg19) ; chr15:g.101646785A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646785A>T , CM000677.2:g.101646785A>T	GRCh38
NC_000015.9:g.102186988A>T , CM000677.1:g.102186988A>T	GRCh37
NC_000015.8:g.100004511A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333202.8:c.442T>A MANE Select	ENSP00000330433.3:p.Ser148Thr
ENST00000333202.7:c.442T>A	ENSP00000330433.3:p.Ser148Thr
ENST00000347970.7:c.364T>A	ENSP00000327584.3:p.Ser122Thr
ENST00000428002.6:c.364T>A	ENSP00000402179.2:p.Ser122Thr
ENST00000558129.5:c.273T>A
ENST00000558677.5:c.743T>A
ENST00000559024.5:n.463T>A
ENST00000559107.5:c.442T>A	ENSP00000454131.1:p.Ser148Thr
ENST00000560013.5:c.*810T>A	ENSP00000453503.1:n.*810T>A
ENST00000560910.5:n.384T>A
ENST00000561373.1:c.247T>A	ENSP00000452823.1:p.Ser83Thr
NM_001307960.1:c.364T>A	NP_001294889.1:p.Ser122Thr
NM_001308026.1:c.442T>A	NP_001294955.1:p.Ser148Thr
NM_025141.3:c.364T>A	NP_079417.2:p.Ser122Thr
NM_078474.2:c.442T>A	NP_510883.2:p.Ser148Thr
NM_078474.3:c.442T>A MANE Select	NP_510883.2:p.Ser148Thr
NM_001307960.2:c.364T>A	NP_001294889.1:p.Ser122Thr
NM_001308026.2:c.442T>A	NP_001294955.1:p.Ser148Thr
NM_025141.4:c.364T>A	NP_079417.2:p.Ser122Thr