Canonical Allele Identifier: CA20294868
Community Standard Title: NM_003680.4(YARS1):c.138C>T (p.Gly46=)
Gene: YARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32810977G>A , CM000663.2:g.32810977G>A GRCh38
NC_000001.10:g.33276578G>A , CM000663.1:g.33276578G>A GRCh37
NC_000001.9:g.33049165G>A NCBI36
NG_008408.1:g.12056C>T , LRG_273:g.12056C>T

Transcript Alleles

HGVS Amino-acid Change
NM_003680.4:c.138C>T MANE Select NP_003671.1:p.Gly46=
ENST00000373477.9:c.138C>T MANE Select ENSP00000362576.4:p.Gly46=
NM_003680.3:c.138C>T , LRG_273t1:c.138C>T NP_003671.1:p.Gly46=
ENST00000373477.8:c.138C>T ENSP00000362576.4:p.Gly46=
ENST00000472692.1:n.671C>T
ENST00000481895.5:n.211C>T
ENST00000481895.6:c.138C>T ENSP00000502016.1:p.Gly46=
ENST00000616261.1:c.138C>T ENSP00000484192.1:p.Gly46=
ENST00000616261.2:c.138C>T ENSP00000484192.2:p.Gly46=
ENST00000674629.1:c.58-4366C>T ENSP00000502470.1:n.58-4366C>T
ENST00000674654.1:c.138C>T ENSP00000501729.1:p.Gly46=
ENST00000675785.1:c.58-211C>T ENSP00000502019.1:n.58-211C>T
ENST00000675785.2:c.58-211C>T ENSP00000502019.1:n.58-211C>T
ENST00000676297.1:c.138C>T ENSP00000501596.1:p.Gly46=
XM_011542347.1:c.-250-4366C>T XP_011540649.1:n.-250-4366C>T
XM_011542347.2:c.-250-4366C>T XP_011540649.1:n.-250-4366C>T
XM_011542348.1:c.-297-4366C>T XP_011540650.1:n.-297-4366C>T
XM_017002651.2:c.-540C>T XP_016858140.1:n.-540C>T