Canonical Allele Identifier: CA2410907651

Gene: TYMP SCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50526148_50526158delinsGGAGAGGGGCT , CM000684.2:g.50526148_50526158delinsGGAGAGGGGCT	GRCh38
NC_000022.10:g.50964577_50964587delinsGGAGAGGGGCT , CM000684.1:g.50964577_50964587delinsGGAGAGGGGCT	GRCh37
NC_000022.9:g.49311443_49311453delinsGGAGAGGGGCT	NCBI36
NG_011860.1:g.8928_8938delinsAGCCCCTCTCC , LRG_727:g.8928_8938delinsAGCCCCTCTCC
NG_016235.1:g.5282_5292delinsAGCCCCTCTCC
NG_021419.1:g.22933_22943delinsGGAGAGGGGCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.1160-17_1160-7delinsAGCCCCTCTCC (TYMP) MANE Select	ENSP00000252029.3:n.1160-17_1160-7delinsA...
ENST00000395680.6:c.1160-17_1160-7delinsAGCCCCTCTCC (TYMP)	ENSP00000379037.1:n.1160-17_1160-7delinsA...
ENST00000395681.6:c.1160-2_1168delinsAGCCCCTCTCC (TYMP)
ENST00000543927.6:c.-14+88_-14+98delinsAGCCCCTCTCC (SCO2)	ENSP00000444433.1:n.-14+88_-14+98delinsAG...
ENST00000651490.1:c.92+88_92+98delinsAGCCCCTCTCC (TYMP)
ENST00000652401.1:c.661-17_661-7delinsAGCCCCTCTCC (TYMP)
ENST00000252029.7:c.1160-17_1160-7delinsAGCCCCTCTCC (TYMP)	ENSP00000252029.3:n.1160-17_1160-7delinsA...
ENST00000395678.7:c.1160-17_1160-7delinsAGCCCCTCTCC (TYMP)	ENSP00000379036.3:n.1160-17_1160-7delinsA...
ENST00000395680.5:c.1160-17_1160-7delinsAGCCCCTCTCC (TYMP)	ENSP00000379037.1:n.1160-17_1160-7delinsA...
ENST00000395681.5:c.1160-2_1168delinsAGCCCCTCTCC (TYMP)
ENST00000423348.1:c.-14+88_-14+98delinsAGCCCCTCTCC	ENSP00000403570.1:n.-14+88_-14+98delinsAG...
ENST00000425169.1:c.1061-17_1061-7delinsAGCCCCTCTCC (TYMP)	ENSP00000395875.1:n.1061-17_1061-7delinsA...
ENST00000476284.1:n.1253_1263delinsAGCCCCTCTCC (TYMP)
ENST00000487577.5:n.1447-17_1447-7delinsAGCCCCTCTCC (TYMP)
ENST00000543927.5:c.-14+88_-14+98delinsAGCCCCTCTCC	ENSP00000444433.1:n.-14+88_-14+98delinsAG...
NM_001113755.2:c.1160-17_1160-7delinsAGCCCCTCTCC (TYMP)	NP_001107227.1:n.1160-17_1160-7delinsAGCC...
NM_001113756.2:c.1160-17_1160-7delinsAGCCCCTCTCC (TYMP)	NP_001107228.1:n.1160-17_1160-7delinsAGCC...
NM_001169109.1:c.-14+88_-14+98delinsAGCCCCTCTCC (SCO2)	NP_001162580.1:n.-14+88_-14+98delinsAGCCC...
NM_001257988.1:c.1160-17_1160-7delinsAGCCCCTCTCC , LRG_727t1:c.1160-17_1160-7delinsAGCCCCTCTCC (TYMP)	NP_001244917.1:n.1160-17_1160-7delinsAGCC...
NM_001257989.1:c.1160-2_1168delinsAGCCCCTCTCC , LRG_727t2:c.1160-2_1168delinsAGCCCCTCTCC (TYMP)
NM_001953.4:c.1160-17_1160-7delinsAGCCCCTCTCC (TYMP)	NP_001944.1:n.1160-17_1160-7delinsAGCCCCT...
NM_001113755.3:c.1160-17_1160-7delinsAGCCCCTCTCC (TYMP)	NP_001107227.1:n.1160-17_1160-7delinsAGCC...
NM_001113756.3:c.1160-17_1160-7delinsAGCCCCTCTCC (TYMP)	NP_001107228.1:n.1160-17_1160-7delinsAGCC...
NM_001953.5:c.1160-17_1160-7delinsAGCCCCTCTCC (TYMP) MANE Select	NP_001944.1:n.1160-17_1160-7delinsAGCCCCT...
NM_001169109.2:c.-14+88_-14+98delinsAGCCCCTCTCC (SCO2)	NP_001162580.1:n.-14+88_-14+98delinsAGCCC...