Canonical Allele Identifier: CA2410907652

Gene: TYMP SCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50526148G= , CM000684.2:g.50526148G=	GRCh38
NC_000022.10:g.50964577G= , CM000684.1:g.50964577G=	GRCh37
NC_000022.9:g.49311443G=	NCBI36
NG_011860.1:g.8938C= , LRG_727:g.8938C=
NG_016235.1:g.5292C=
NG_021419.1:g.22933G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.1160-7C= (TYMP) MANE Select	ENSP00000252029.3:n.1160-7C=
ENST00000395680.6:c.1160-7C= (TYMP)	ENSP00000379037.1:n.1160-7C=
ENST00000395681.6:c.1168C= (TYMP)	ENSP00000379038.1:p.Pro390=
ENST00000543927.6:c.-14+98C= (SCO2)	ENSP00000444433.1:n.-14+98C=
ENST00000651490.1:c.92+98C= (TYMP)
ENST00000652401.1:c.661-7C= (TYMP)
ENST00000252029.7:c.1160-7C= (TYMP)	ENSP00000252029.3:n.1160-7C=
ENST00000395678.7:c.1160-7C= (TYMP)	ENSP00000379036.3:n.1160-7C=
ENST00000395680.5:c.1160-7C= (TYMP)	ENSP00000379037.1:n.1160-7C=
ENST00000395681.5:c.1168C= (TYMP)	ENSP00000379038.1:p.Pro390=
ENST00000423348.1:c.-14+98C=	ENSP00000403570.1:n.-14+98C=
ENST00000425169.1:c.1061-7C= (TYMP)	ENSP00000395875.1:n.1061-7C=
ENST00000476284.1:n.1263C= (TYMP)
ENST00000487577.5:n.1447-7C= (TYMP)
ENST00000543927.5:c.-14+98C=	ENSP00000444433.1:n.-14+98C=
NM_001113755.2:c.1160-7C= (TYMP)	NP_001107227.1:n.1160-7C=
NM_001113756.2:c.1160-7C= (TYMP)	NP_001107228.1:n.1160-7C=
NM_001169109.1:c.-14+98C= (SCO2)	NP_001162580.1:n.-14+98C=
NM_001257988.1:c.1160-7C= , LRG_727t1:c.1160-7C= (TYMP)	NP_001244917.1:n.1160-7C=
NM_001257989.1:c.1168C= , LRG_727t2:c.1168C= (TYMP)	NP_001244918.1:p.Pro390=
NM_001953.4:c.1160-7C= (TYMP)	NP_001944.1:n.1160-7C=
NM_001113755.3:c.1160-7C= (TYMP)	NP_001107227.1:n.1160-7C=
NM_001113756.3:c.1160-7C= (TYMP)	NP_001107228.1:n.1160-7C=
NM_001953.5:c.1160-7C= (TYMP) MANE Select	NP_001944.1:n.1160-7C=
NM_001169109.2:c.-14+98C= (SCO2)	NP_001162580.1:n.-14+98C=