Canonical Allele Identifier: CA492691469

Gene: TM2D3

Linked Data

• MyVariant Identifiers: chr15:g.102186947C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646744C>A , CM000677.2:g.101646744C>A	GRCh38
NC_000015.9:g.102186947C>A , CM000677.1:g.102186947C>A	GRCh37
NC_000015.8:g.100004470C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333202.8:c.483G>T MANE Select	ENSP00000330433.3:p.Arg161=
ENST00000333202.7:c.483G>T	ENSP00000330433.3:p.Arg161=
ENST00000347970.7:c.405G>T	ENSP00000327584.3:p.Arg135=
ENST00000428002.6:c.405G>T	ENSP00000402179.2:p.Arg135=
ENST00000558129.5:c.314G>T
ENST00000558677.5:c.784G>T
ENST00000559024.5:n.504G>T
ENST00000559107.5:c.483G>T	ENSP00000454131.1:p.Arg161=
ENST00000560013.5:c.*851G>T	ENSP00000453503.1:n.*851G>T
ENST00000560910.5:n.425G>T
ENST00000561373.1:c.288G>T	ENSP00000452823.1:p.Arg96=
NM_001307960.1:c.405G>T	NP_001294889.1:p.Arg135=
NM_001308026.1:c.483G>T	NP_001294955.1:p.Arg161=
NM_025141.3:c.405G>T	NP_079417.2:p.Arg135=
NM_078474.2:c.483G>T	NP_510883.2:p.Arg161=
NM_078474.3:c.483G>T MANE Select	NP_510883.2:p.Arg161=
NM_001307960.2:c.405G>T	NP_001294889.1:p.Arg135=
NM_001308026.2:c.483G>T	NP_001294955.1:p.Arg161=
NM_025141.4:c.405G>T	NP_079417.2:p.Arg135=