Canonical Allele Identifier: CA2410907650

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50526146G= , CM000684.2:g.50526146G= GRCh38
NC_000022.10:g.50964575G= , CM000684.1:g.50964575G= GRCh37
NC_000022.9:g.49311441G= NCBI36
NG_011860.1:g.8940C= , LRG_727:g.8940C=
NG_016235.1:g.5294C=
NG_021419.1:g.22931G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.1160-5C= (TYMP) MANE Select ENSP00000252029.3:n.1160-5C=
ENST00000395680.6:c.1160-5C= (TYMP) ENSP00000379037.1:n.1160-5C=
ENST00000395681.6:c.1170C= (TYMP) ENSP00000379038.1:p.Pro390=
ENST00000543927.6:c.-14+100C= (SCO2) ENSP00000444433.1:n.-14+100C=
ENST00000651490.1:c.92+100C= (TYMP)
ENST00000652401.1:c.661-5C= (TYMP)
ENST00000252029.7:c.1160-5C= (TYMP) ENSP00000252029.3:n.1160-5C=
ENST00000395678.7:c.1160-5C= (TYMP) ENSP00000379036.3:n.1160-5C=
ENST00000395680.5:c.1160-5C= (TYMP) ENSP00000379037.1:n.1160-5C=
ENST00000395681.5:c.1170C= (TYMP) ENSP00000379038.1:p.Pro390=
ENST00000423348.1:c.-14+100C= ENSP00000403570.1:n.-14+100C=
ENST00000425169.1:c.1061-5C= (TYMP) ENSP00000395875.1:n.1061-5C=
ENST00000476284.1:n.1265C= (TYMP)
ENST00000487577.5:n.1447-5C= (TYMP)
ENST00000543927.5:c.-14+100C= ENSP00000444433.1:n.-14+100C=
NM_001113755.2:c.1160-5C= (TYMP) NP_001107227.1:n.1160-5C=
NM_001113756.2:c.1160-5C= (TYMP) NP_001107228.1:n.1160-5C=
NM_001169109.1:c.-14+100C= (SCO2) NP_001162580.1:n.-14+100C=
NM_001257988.1:c.1160-5C= , LRG_727t1:c.1160-5C= (TYMP) NP_001244917.1:n.1160-5C=
NM_001257989.1:c.1170C= , LRG_727t2:c.1170C= (TYMP) NP_001244918.1:p.Pro390=
NM_001953.4:c.1160-5C= (TYMP) NP_001944.1:n.1160-5C=
NM_001113755.3:c.1160-5C= (TYMP) NP_001107227.1:n.1160-5C=
NM_001113756.3:c.1160-5C= (TYMP) NP_001107228.1:n.1160-5C=
NM_001953.5:c.1160-5C= (TYMP) MANE Select NP_001944.1:n.1160-5C=
NM_001169109.2:c.-14+100C= (SCO2) NP_001162580.1:n.-14+100C=