Canonical Allele Identifier: CA2595597052
Gene: YARS1 HGNC NCBI

Linked Data

dbSNP Id: rs2148616754
gnomAD v3: 1-32811109-T-A
gnomAD v4: 1-32811109-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32811109T>A , CM000663.2:g.32811109T>A GRCh38
NC_000001.10:g.33276710T>A , CM000663.1:g.33276710T>A GRCh37
NC_000001.9:g.33049297T>A NCBI36
NG_008408.1:g.11924A>T , LRG_273:g.11924A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.58-343A>T ENSP00000502019.1:n.58-343A>T
ENST00000373477.9:c.58-52A>T MANE Select ENSP00000362576.4:n.58-52A>T
ENST00000481895.6:c.58-52A>T ENSP00000502016.1:n.58-52A>T
ENST00000616261.2:c.58-52A>T ENSP00000484192.2:n.58-52A>T
ENST00000674629.1:c.58-4498A>T ENSP00000502470.1:n.58-4498A>T
ENST00000674654.1:c.58-52A>T ENSP00000501729.1:n.58-52A>T
ENST00000675785.1:c.58-343A>T ENSP00000502019.1:n.58-343A>T
ENST00000676297.1:c.58-52A>T ENSP00000501596.1:n.58-52A>T
ENST00000373477.8:c.58-52A>T ENSP00000362576.4:n.58-52A>T
ENST00000472692.1:n.539A>T
ENST00000481895.5:n.131-52A>T
ENST00000616261.1:c.58-52A>T ENSP00000484192.1:n.58-52A>T
NM_003680.3:c.58-52A>T , LRG_273t1:c.58-52A>T NP_003671.1:n.58-52A>T
XM_011542347.1:c.-250-4498A>T XP_011540649.1:n.-250-4498A>T
XM_011542348.1:c.-297-4498A>T XP_011540650.1:n.-297-4498A>T
XM_011542347.2:c.-250-4498A>T XP_011540649.1:n.-250-4498A>T
XM_017002651.2:c.-620-52A>T XP_016858140.1:n.-620-52A>T
NM_003680.4:c.58-52A>T MANE Select NP_003671.1:n.58-52A>T