Canonical Allele Identifier: CA492691497

Gene: TM2D3

Linked Data

• MyVariant Identifiers: chr15:g.102186977C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646774C>G , CM000677.2:g.101646774C>G	GRCh38
NC_000015.9:g.102186977C>G , CM000677.1:g.102186977C>G	GRCh37
NC_000015.8:g.100004500C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000333202.8:c.453G>C MANE Select	ENSP00000330433.3:p.Arg151=
ENST00000333202.7:c.453G>C	ENSP00000330433.3:p.Arg151=
ENST00000347970.7:c.375G>C	ENSP00000327584.3:p.Arg125=
ENST00000428002.6:c.375G>C	ENSP00000402179.2:p.Arg125=
ENST00000558129.5:c.284G>C
ENST00000558677.5:c.754G>C
ENST00000559024.5:n.474G>C
ENST00000559107.5:c.453G>C	ENSP00000454131.1:p.Arg151=
ENST00000560013.5:c.*821G>C	ENSP00000453503.1:n.*821G>C
ENST00000560910.5:n.395G>C
ENST00000561373.1:c.258G>C	ENSP00000452823.1:p.Arg86=
NM_001307960.1:c.375G>C	NP_001294889.1:p.Arg125=
NM_001308026.1:c.453G>C	NP_001294955.1:p.Arg151=
NM_025141.3:c.375G>C	NP_079417.2:p.Arg125=
NM_078474.2:c.453G>C	NP_510883.2:p.Arg151=
NM_078474.3:c.453G>C MANE Select	NP_510883.2:p.Arg151=
NM_001307960.2:c.375G>C	NP_001294889.1:p.Arg125=
NM_001308026.2:c.453G>C	NP_001294955.1:p.Arg151=
NM_025141.4:c.375G>C	NP_079417.2:p.Arg125=