Canonical Allele Identifier: CA2200628484

Gene: TM2D3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646763G= , CM000677.2:g.101646763G=	GRCh38
NC_000015.9:g.102186966G= , CM000677.1:g.102186966G=	GRCh37
NC_000015.8:g.100004489G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333202.8:c.464C= MANE Select	ENSP00000330433.3:p.Pro155=
ENST00000333202.7:c.464C=	ENSP00000330433.3:p.Pro155=
ENST00000347970.7:c.386C=	ENSP00000327584.3:p.Pro129=
ENST00000428002.6:c.386C=	ENSP00000402179.2:p.Pro129=
ENST00000558129.5:c.295C=
ENST00000558677.5:c.765C=
ENST00000559024.5:n.485C=
ENST00000559107.5:c.464C=	ENSP00000454131.1:p.Pro155=
ENST00000560013.5:c.*832C=	ENSP00000453503.1:n.*832C=
ENST00000560910.5:n.406C=
ENST00000561373.1:c.269C=	ENSP00000452823.1:p.Pro90=
NM_001307960.1:c.386C=	NP_001294889.1:p.Pro129=
NM_001308026.1:c.464C=	NP_001294955.1:p.Pro155=
NM_025141.3:c.386C=	NP_079417.2:p.Pro129=
NM_078474.2:c.464C=	NP_510883.2:p.Pro155=
NM_078474.3:c.464C= MANE Select	NP_510883.2:p.Pro155=
NM_001307960.2:c.386C=	NP_001294889.1:p.Pro129=
NM_001308026.2:c.464C=	NP_001294955.1:p.Pro155=
NM_025141.4:c.386C=	NP_079417.2:p.Pro129=