Canonical Allele Identifier: CA2473063236
Gene: YARS1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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