Canonical Allele Identifier: CA2473076885
Gene: YARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32811007A= , CM000663.2:g.32811007A= GRCh38
NC_000001.10:g.33276608A= , CM000663.1:g.33276608A= GRCh37
NC_000001.9:g.33049195A= NCBI36
NG_008408.1:g.12026T= , LRG_273:g.12026T=

Transcript Alleles

HGVS Amino-acid change
ENST00000675785.2:c.58-241T= ENSP00000502019.1:n.58-241T=
ENST00000373477.9:c.108T= MANE Select ENSP00000362576.4:p.Leu36=
ENST00000481895.6:c.108T= ENSP00000502016.1:p.Leu36=
ENST00000616261.2:c.108T= ENSP00000484192.2:p.Leu36=
ENST00000674629.1:c.58-4396T= ENSP00000502470.1:n.58-4396T=
ENST00000674654.1:c.108T= ENSP00000501729.1:p.Leu36=
ENST00000675785.1:c.58-241T= ENSP00000502019.1:n.58-241T=
ENST00000676297.1:c.108T= ENSP00000501596.1:p.Leu36=
ENST00000373477.8:c.108T= ENSP00000362576.4:p.Leu36=
ENST00000472692.1:n.641T=
ENST00000481895.5:n.181T=
ENST00000616261.1:c.108T= ENSP00000484192.1:p.Leu36=
NM_003680.3:c.108T= , LRG_273t1:c.108T= NP_003671.1:p.Leu36=
XM_011542347.1:c.-250-4396T= XP_011540649.1:n.-250-4396T=
XM_011542348.1:c.-297-4396T= XP_011540650.1:n.-297-4396T=
XM_011542347.2:c.-250-4396T= XP_011540649.1:n.-250-4396T=
XM_017002651.2:c.-570T= XP_016858140.1:n.-570T=
NM_003680.4:c.108T= MANE Select NP_003671.1:p.Leu36=