Canonical Allele Identifier: CA2410907481

Gene: TYMP SCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50525919C= , CM000684.2:g.50525919C=	GRCh38
NC_000022.10:g.50964348C= , CM000684.1:g.50964348C=	GRCh37
NC_000022.9:g.49311214C=	NCBI36
NG_011860.1:g.9167G= , LRG_727:g.9167G=
NG_016235.1:g.5521G=
NG_021419.1:g.22704C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.1301-1G= (TYMP) MANE Select	ENSP00000252029.3:n.1301-1G=
ENST00000395680.6:c.1301-1G= (TYMP)	ENSP00000379037.1:n.1301-1G=
ENST00000395681.6:c.1316-1G= (TYMP)	ENSP00000379038.1:n.1316-1G=
ENST00000543927.6:c.-14+327G= (SCO2)	ENSP00000444433.1:n.-14+327G=
ENST00000638598.2:c.-14+82G= (SCO2)	ENSP00000491753.2:n.-14+82G=
ENST00000651490.1:c.93-1G= (TYMP)
ENST00000652401.1:c.802-1G= (TYMP)
ENST00000252029.7:c.1301-1G= (TYMP)	ENSP00000252029.3:n.1301-1G=
ENST00000395678.7:c.1301-1G= (TYMP)	ENSP00000379036.3:n.1301-1G=
ENST00000395680.5:c.1301-1G= (TYMP)	ENSP00000379037.1:n.1301-1G=
ENST00000395681.5:c.1316-1G= (TYMP)	ENSP00000379038.1:n.1316-1G=
ENST00000423348.1:c.-14+327G=	ENSP00000403570.1:n.-14+327G=
ENST00000425169.1:c.1202-1G= (TYMP)	ENSP00000395875.1:n.1202-1G=
ENST00000439934.5:c.-14+82G=	ENSP00000415642.1:n.-14+82G=
ENST00000476284.1:n.1411-1G= (TYMP)
ENST00000487577.5:n.1588-1G= (TYMP)
ENST00000535425.5:c.-14+82G=	ENSP00000444242.1:n.-14+82G=
ENST00000543927.5:c.-14+327G=	ENSP00000444433.1:n.-14+327G=
NM_001113755.2:c.1301-1G= (TYMP)	NP_001107227.1:n.1301-1G=
NM_001113756.2:c.1301-1G= (TYMP)	NP_001107228.1:n.1301-1G=
NM_001169109.1:c.-14+327G= (SCO2)	NP_001162580.1:n.-14+327G=
NM_001169110.1:c.-14+82G= (SCO2)	NP_001162581.1:n.-14+82G=
NM_001257988.1:c.1301-1G= , LRG_727t1:c.1301-1G= (TYMP)	NP_001244917.1:n.1301-1G=
NM_001257989.1:c.1316-1G= , LRG_727t2:c.1316-1G= (TYMP)	NP_001244918.1:n.1316-1G=
NM_001953.4:c.1301-1G= (TYMP)	NP_001944.1:n.1301-1G=
NM_001113755.3:c.1301-1G= (TYMP)	NP_001107227.1:n.1301-1G=
NM_001113756.3:c.1301-1G= (TYMP)	NP_001107228.1:n.1301-1G=
NM_001953.5:c.1301-1G= (TYMP) MANE Select	NP_001944.1:n.1301-1G=
NM_001169109.2:c.-14+327G= (SCO2)	NP_001162580.1:n.-14+327G=