Canonical Allele Identifier: CA325560569

Linked Data

dbSNP Id: rs748559929

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50526241C>G , CM000684.2:g.50526241C>G GRCh38
NC_000022.10:g.50964670C>G , CM000684.1:g.50964670C>G GRCh37
NC_000022.9:g.49311536C>G NCBI36
NG_011860.1:g.8845G>C , LRG_727:g.8845G>C
NG_016235.1:g.5199G>C
NG_021419.1:g.23026C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.1159+5G>C (TYMP) MANE Select ENSP00000252029.3:n.1159+5G>C
ENST00000395680.6:c.1159+5G>C (TYMP) ENSP00000379037.1:n.1159+5G>C
ENST00000395681.6:c.1159+5G>C (TYMP) ENSP00000379038.1:n.1159+5G>C
ENST00000543927.6:c.-14+5G>C (SCO2) ENSP00000444433.1:n.-14+5G>C
ENST00000651490.1:c.92+5G>C (TYMP)
ENST00000652401.1:c.660+5G>C (TYMP)
ENST00000252029.7:c.1159+5G>C (TYMP) ENSP00000252029.3:n.1159+5G>C
ENST00000395678.7:c.1159+5G>C (TYMP) ENSP00000379036.3:n.1159+5G>C
ENST00000395680.5:c.1159+5G>C (TYMP) ENSP00000379037.1:n.1159+5G>C
ENST00000395681.5:c.1159+5G>C (TYMP) ENSP00000379038.1:n.1159+5G>C
ENST00000423348.1:c.-14+5G>C ENSP00000403570.1:n.-14+5G>C
ENST00000425169.1:c.1060+5G>C (TYMP) ENSP00000395875.1:n.1060+5G>C
ENST00000476284.1:n.1170G>C (TYMP)
ENST00000487577.5:n.1446+5G>C (TYMP)
ENST00000543927.5:c.-14+5G>C ENSP00000444433.1:n.-14+5G>C
NM_001113755.2:c.1159+5G>C (TYMP) NP_001107227.1:n.1159+5G>C
NM_001113756.2:c.1159+5G>C (TYMP) NP_001107228.1:n.1159+5G>C
NM_001169109.1:c.-14+5G>C (SCO2) NP_001162580.1:n.-14+5G>C
NM_001257988.1:c.1159+5G>C , LRG_727t1:c.1159+5G>C (TYMP) NP_001244917.1:n.1159+5G>C
NM_001257989.1:c.1159+5G>C , LRG_727t2:c.1159+5G>C (TYMP) NP_001244918.1:n.1159+5G>C
NM_001953.4:c.1159+5G>C (TYMP) NP_001944.1:n.1159+5G>C
NM_001113755.3:c.1159+5G>C (TYMP) NP_001107227.1:n.1159+5G>C
NM_001113756.3:c.1159+5G>C (TYMP) NP_001107228.1:n.1159+5G>C
NM_001953.5:c.1159+5G>C (TYMP) MANE Select NP_001944.1:n.1159+5G>C
NM_001169109.2:c.-14+5G>C (SCO2) NP_001162580.1:n.-14+5G>C