Canonical Allele Identifier: CA2644702472
Gene: YARS1 HGNC NCBI

Linked Data

gnomAD v4: 1-32779991-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32779991T>C , CM000663.2:g.32779991T>C GRCh38
NC_000001.10:g.33245592T>C , CM000663.1:g.33245592T>C GRCh37
NC_000001.9:g.33018179T>C NCBI36
NG_008408.1:g.43042A>G , LRG_273:g.43042A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.1187+94A>G ENSP00000502019.1:n.1187+94A>G
ENST00000373477.9:c.1334+94A>G MANE Select ENSP00000362576.4:n.1334+94A>G
ENST00000674629.1:c.*882+94A>G ENSP00000502470.1:n.*882+94A>G
ENST00000674654.1:c.*1294+94A>G ENSP00000501729.1:n.*1294+94A>G
ENST00000675785.1:c.1187+94A>G ENSP00000502019.1:n.1187+94A>G
ENST00000676297.1:c.*1508+94A>G ENSP00000501596.1:n.*1508+94A>G
ENST00000373477.8:c.1334+94A>G ENSP00000362576.4:n.1334+94A>G
ENST00000469100.5:n.1250+94A>G
ENST00000478828.1:n.801+94A>G
ENST00000487404.5:n.1644+94A>G
ENST00000490826.1:n.721A>G
NM_003680.3:c.1334+94A>G , LRG_273t1:c.1334+94A>G NP_003671.1:n.1334+94A>G
XM_011542347.1:c.704+94A>G XP_011540649.1:n.704+94A>G
XM_011542348.1:c.704+94A>G XP_011540650.1:n.704+94A>G
XM_011542347.2:c.704+94A>G XP_011540649.1:n.704+94A>G
XM_017002651.2:c.704+94A>G XP_016858140.1:n.704+94A>G
NM_003680.4:c.1334+94A>G MANE Select NP_003671.1:n.1334+94A>G