Canonical Allele Identifier: CA2805490154

Gene: TM2D3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646675A>C , CM000677.2:g.101646675A>C	GRCh38
NC_000015.9:g.102186878A>C , CM000677.1:g.102186878A>C	GRCh37
NC_000015.8:g.100004401A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333202.8:c.502+50T>G MANE Select	ENSP00000330433.3:n.502+50T>G
ENST00000333202.7:c.502+50T>G	ENSP00000330433.3:n.502+50T>G
ENST00000347970.7:c.424+50T>G	ENSP00000327584.3:n.424+50T>G
ENST00000428002.6:c.424+50T>G	ENSP00000402179.2:n.424+50T>G
ENST00000558129.5:c.333+50T>G
ENST00000558677.5:c.803+50T>G
ENST00000559024.5:n.573T>G
ENST00000559107.5:c.502+50T>G	ENSP00000454131.1:n.502+50T>G
ENST00000560013.5:c.*870+50T>G	ENSP00000453503.1:n.*870+50T>G
ENST00000560910.5:n.494T>G
ENST00000561373.1:c.307+50T>G	ENSP00000452823.1:n.307+50T>G
NM_001307960.1:c.424+50T>G	NP_001294889.1:n.424+50T>G
NM_001308026.1:c.502+50T>G	NP_001294955.1:n.502+50T>G
NM_025141.3:c.424+50T>G	NP_079417.2:n.424+50T>G
NM_078474.2:c.502+50T>G	NP_510883.2:n.502+50T>G
NM_078474.3:c.502+50T>G MANE Select	NP_510883.2:n.502+50T>G
NM_001307960.2:c.424+50T>G	NP_001294889.1:n.424+50T>G
NM_001308026.2:c.502+50T>G	NP_001294955.1:n.502+50T>G
NM_025141.4:c.424+50T>G	NP_079417.2:n.424+50T>G