Canonical Allele Identifier: CA16616796

Linked Data

ClinVar Variation Id: 223054
ClinVar RCV Id: RCV000208687
dbSNP Id: rs1064792873

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50526141C>T , CM000684.2:g.50526141C>T GRCh38
NC_000022.10:g.50964570C>T , CM000684.1:g.50964570C>T GRCh37
NC_000022.9:g.49311436C>T NCBI36
NG_011860.1:g.8945G>A , LRG_727:g.8945G>A
NG_016235.1:g.5299G>A
NG_021419.1:g.22926C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.1160G>A (TYMP) MANE Select ENSP00000252029.3:p.Gly387Asp
ENST00000395680.6:c.1160G>A (TYMP) ENSP00000379037.1:p.Gly387Asp
ENST00000395681.6:c.1175G>A (TYMP) ENSP00000379038.1:p.Gly392Asp
ENST00000543927.6:c.-14+105G>A (SCO2) ENSP00000444433.1:n.-14+105G>A
ENST00000638598.2:c.-154G>A (SCO2) ENSP00000491753.2:n.-154G>A
ENST00000651490.1:c.92+105G>A (TYMP)
ENST00000652401.1:c.661G>A (TYMP)
ENST00000252029.7:c.1160G>A (TYMP) ENSP00000252029.3:p.Gly387Asp
ENST00000395678.7:c.1160G>A (TYMP) ENSP00000379036.3:p.Gly387Asp
ENST00000395680.5:c.1160G>A (TYMP) ENSP00000379037.1:p.Gly387Asp
ENST00000395681.5:c.1175G>A (TYMP) ENSP00000379038.1:p.Gly392Asp
ENST00000423348.1:c.-14+105G>A ENSP00000403570.1:n.-14+105G>A
ENST00000425169.1:c.1061G>A (TYMP) ENSP00000395875.1:p.Gly354Asp
ENST00000439934.5:c.-154G>A ENSP00000415642.1:n.-154G>A
ENST00000476284.1:n.1270G>A (TYMP)
ENST00000487577.5:n.1447G>A (TYMP)
ENST00000535425.5:c.-154G>A ENSP00000444242.1:n.-154G>A
ENST00000543927.5:c.-14+105G>A ENSP00000444433.1:n.-14+105G>A
NM_001113755.2:c.1160G>A (TYMP) NP_001107227.1:p.Gly387Asp
NM_001113756.2:c.1160G>A (TYMP) NP_001107228.1:p.Gly387Asp
NM_001169109.1:c.-14+105G>A (SCO2) NP_001162580.1:n.-14+105G>A
NM_001169110.1:c.-154G>A (SCO2) NP_001162581.1:n.-154G>A
NM_001257988.1:c.1160G>A , LRG_727t1:c.1160G>A (TYMP) NP_001244917.1:p.Gly387Asp
NM_001257989.1:c.1175G>A , LRG_727t2:c.1175G>A (TYMP) NP_001244918.1:p.Gly392Asp
NM_001953.4:c.1160G>A (TYMP) NP_001944.1:p.Gly387Asp
NM_001113755.3:c.1160G>A (TYMP) NP_001107227.1:p.Gly387Asp
NM_001113756.3:c.1160G>A (TYMP) NP_001107228.1:p.Gly387Asp
NM_001953.5:c.1160G>A (TYMP) MANE Select NP_001944.1:p.Gly387Asp
NM_001169109.2:c.-14+105G>A (SCO2) NP_001162580.1:n.-14+105G>A