Canonical Allele Identifier: CA339687260
Gene: YARS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.33276311C>T (hg19) chr1:g.32810710C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32810710C>T , CM000663.2:g.32810710C>T GRCh38
NC_000001.10:g.33276311C>T , CM000663.1:g.33276311C>T GRCh37
NC_000001.9:g.33048898C>T NCBI36
NG_008408.1:g.12323G>A , LRG_273:g.12323G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000675785.2:c.114G>A ENSP00000502019.1:p.Trp38Ter
ENST00000373477.9:c.261G>A MANE Select ENSP00000362576.4:p.Trp87Ter
ENST00000481895.6:c.261G>A ENSP00000502016.1:p.Trp87Ter
ENST00000616261.2:c.261G>A ENSP00000484192.2:p.Trp87Ter
ENST00000674629.1:c.58-4099G>A ENSP00000502470.1:n.58-4099G>A
ENST00000674654.1:c.261G>A ENSP00000501729.1:p.Trp87Ter
ENST00000675785.1:c.114G>A ENSP00000502019.1:p.Trp38Ter
ENST00000676297.1:c.261G>A ENSP00000501596.1:p.Trp87Ter
ENST00000373477.8:c.261G>A ENSP00000362576.4:p.Trp87Ter
ENST00000481895.5:n.334G>A
ENST00000616261.1:c.261G>A ENSP00000484192.1:p.Trp87Ter
NM_003680.3:c.261G>A , LRG_273t1:c.261G>A NP_003671.1:p.Trp87Ter
XM_011542347.1:c.-250-4099G>A XP_011540649.1:n.-250-4099G>A
XM_011542348.1:c.-297-4099G>A XP_011540650.1:n.-297-4099G>A
XM_011542347.2:c.-250-4099G>A XP_011540649.1:n.-250-4099G>A
XM_017002651.2:c.-417G>A XP_016858140.1:n.-417G>A
NM_003680.4:c.261G>A MANE Select NP_003671.1:p.Trp87Ter
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