Canonical Allele Identifier: CA2473063237
Gene: YARS1 HGNC NCBI

Linked Data

dbSNP Id: rs1569707502

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780350T>C , CM000663.2:g.32780350T>C GRCh38
NC_000001.10:g.33245951T>C , CM000663.1:g.33245951T>C GRCh37
NC_000001.9:g.33018538T>C NCBI36
NG_008408.1:g.42683A>G , LRG_273:g.42683A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.994-72A>G ENSP00000502019.1:n.994-72A>G
ENST00000373477.9:c.1141-72A>G MANE Select ENSP00000362576.4:n.1141-72A>G
ENST00000674629.1:c.*689-72A>G ENSP00000502470.1:n.*689-72A>G
ENST00000674654.1:c.*1101-72A>G ENSP00000501729.1:n.*1101-72A>G
ENST00000675785.1:c.994-72A>G ENSP00000502019.1:n.994-72A>G
ENST00000676297.1:c.*1315-72A>G ENSP00000501596.1:n.*1315-72A>G
ENST00000373477.8:c.1141-72A>G ENSP00000362576.4:n.1141-72A>G
ENST00000469100.5:n.1057-72A>G
ENST00000478828.1:n.608-72A>G
ENST00000487404.5:n.1451-72A>G
ENST00000490826.1:n.362A>G
ENST00000616261.1:c.1140-72A>G ENSP00000484192.1:n.1140-72A>G
NM_003680.3:c.1141-72A>G , LRG_273t1:c.1141-72A>G NP_003671.1:n.1141-72A>G
XM_011542347.1:c.511-72A>G XP_011540649.1:n.511-72A>G
XM_011542348.1:c.511-72A>G XP_011540650.1:n.511-72A>G
XM_011542347.2:c.511-72A>G XP_011540649.1:n.511-72A>G
XM_017002651.2:c.511-72A>G XP_016858140.1:n.511-72A>G
NM_003680.4:c.1141-72A>G MANE Select NP_003671.1:n.1141-72A>G