Canonical Allele Identifier: CA2410907440

Gene: TYMP SCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50525867_50525889delinsTGCGGGCCGCTGAGCGCGGGGCC , CM000684.2:g.50525867_50525889delinsTGCGGGCCGCTGAGCGCGGGGCC	GRCh38
NC_000022.10:g.50964296_50964318delinsTGCGGGCCGCTGAGCGCGGGGCC , CM000684.1:g.50964296_50964318delinsTGCGGGCCGCTGAGCGCGGGGCC	GRCh37
NC_000022.9:g.49311162_49311184delinsTGCGGGCCGCTGAGCGCGGGGCC	NCBI36
NG_011860.1:g.9197_9219delinsGGCCCCGCGCTCAGCGGCCCGCA , LRG_727:g.9197_9219delinsGGCCCCGCGCTCAGCGGCCCGCA
NG_016235.1:g.5551_5573delinsGGCCCCGCGCTCAGCGGCCCGCA
NG_021419.1:g.22652_22674delinsTGCGGGCCGCTGAGCGCGGGGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP) MANE Select	ENSP00000252029.3:p.Gly444=
ENST00000395680.6:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	ENSP00000379037.1:p.Gly444=
ENST00000395681.6:c.1345_1367delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	ENSP00000379038.1:p.Gly449=
ENST00000543927.6:c.-14+357_-14+379delinsGGCCCCGCGCTCAGCGGCCCGCA (SCO2)	ENSP00000444433.1:n.-14+357_-14+379delins...
ENST00000638598.2:c.-14+112_-14+134delinsGGCCCCGCGCTCAGCGGCCCGCA (SCO2)	ENSP00000491753.2:n.-14+112_-14+134delins...
ENST00000651490.1:c.122_144delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)
ENST00000652401.1:c.831_853delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)
ENST00000252029.7:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	ENSP00000252029.3:p.Gly444=
ENST00000395678.7:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	ENSP00000379036.3:p.Gly444=
ENST00000395680.5:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	ENSP00000379037.1:p.Gly444=
ENST00000395681.5:c.1345_1367delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	ENSP00000379038.1:p.Gly449=
ENST00000423348.1:c.-14+357_-14+379delinsGGCCCCGCGCTCAGCGGCCCGCA	ENSP00000403570.1:n.-14+357_-14+379delins...
ENST00000425169.1:c.1231_1253delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	ENSP00000395875.1:p.Gly411=
ENST00000439934.5:c.-14+112_-14+134delinsGGCCCCGCGCTCAGCGGCCCGCA	ENSP00000415642.1:n.-14+112_-14+134delins...
ENST00000476284.1:n.1440_1462delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)
ENST00000487577.5:n.1617_1639delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)
ENST00000535425.5:c.-14+112_-14+134delinsGGCCCCGCGCTCAGCGGCCCGCA	ENSP00000444242.1:n.-14+112_-14+134delins...
ENST00000543927.5:c.-14+357_-14+379delinsGGCCCCGCGCTCAGCGGCCCGCA	ENSP00000444433.1:n.-14+357_-14+379delins...
NM_001113755.2:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	NP_001107227.1:p.Gly444=
NM_001113756.2:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	NP_001107228.1:p.Gly444=
NM_001169109.1:c.-14+357_-14+379delinsGGCCCCGCGCTCAGCGGCCCGCA (SCO2)	NP_001162580.1:n.-14+357_-14+379delinsGGC...
NM_001169110.1:c.-14+112_-14+134delinsGGCCCCGCGCTCAGCGGCCCGCA (SCO2)	NP_001162581.1:n.-14+112_-14+134delinsGGC...
NM_001257988.1:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA , LRG_727t1:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	NP_001244917.1:p.Gly444=
NM_001257989.1:c.1345_1367delinsGGCCCCGCGCTCAGCGGCCCGCA , LRG_727t2:c.1345_1367delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	NP_001244918.1:p.Gly449=
NM_001953.4:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	NP_001944.1:p.Gly444=
NM_001113755.3:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	NP_001107227.1:p.Gly444=
NM_001113756.3:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP)	NP_001107228.1:p.Gly444=
NM_001953.5:c.1330_1352delinsGGCCCCGCGCTCAGCGGCCCGCA (TYMP) MANE Select	NP_001944.1:p.Gly444=
NM_001169109.2:c.-14+357_-14+379delinsGGCCCCGCGCTCAGCGGCCCGCA (SCO2)	NP_001162580.1:n.-14+357_-14+379delinsGGC...