Canonical Allele Identifier: CA2574301838

Gene: YARS1

Linked Data

• gnomAD v4: 1-32780307-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780307G>A , CM000663.2:g.32780307G>A	GRCh38
NC_000001.10:g.33245908G>A , CM000663.1:g.33245908G>A	GRCh37
NC_000001.9:g.33018495G>A	NCBI36
NG_008408.1:g.42726C>T , LRG_273:g.42726C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.994-29C>T	ENSP00000502019.1:n.994-29C>T
ENST00000373477.9:c.1141-29C>T MANE Select	ENSP00000362576.4:n.1141-29C>T
ENST00000674629.1:c.*689-29C>T	ENSP00000502470.1:n.*689-29C>T
ENST00000674654.1:c.*1101-29C>T	ENSP00000501729.1:n.*1101-29C>T
ENST00000675785.1:c.994-29C>T	ENSP00000502019.1:n.994-29C>T
ENST00000676297.1:c.*1315-29C>T	ENSP00000501596.1:n.*1315-29C>T
ENST00000373477.8:c.1141-29C>T	ENSP00000362576.4:n.1141-29C>T
ENST00000469100.5:n.1057-29C>T
ENST00000478828.1:n.608-29C>T
ENST00000487404.5:n.1451-29C>T
ENST00000490826.1:n.405C>T
ENST00000616261.1:c.1140-29C>T	ENSP00000484192.1:n.1140-29C>T
NM_003680.3:c.1141-29C>T , LRG_273t1:c.1141-29C>T	NP_003671.1:n.1141-29C>T
XM_011542347.1:c.511-29C>T	XP_011540649.1:n.511-29C>T
XM_011542348.1:c.511-29C>T	XP_011540650.1:n.511-29C>T
XM_011542347.2:c.511-29C>T	XP_011540649.1:n.511-29C>T
XM_017002651.2:c.511-29C>T	XP_016858140.1:n.511-29C>T
NM_003680.4:c.1141-29C>T MANE Select	NP_003671.1:n.1141-29C>T