Canonical Allele Identifier: CA2233454835
Gene: KARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.75636503A= , CM000678.2:g.75636503A= GRCh38
NC_000016.9:g.75670401A= , CM000678.1:g.75670401A= GRCh37
NC_000016.8:g.74227902A= NCBI36
NG_028025.1:g.16185T= , LRG_366:g.16185T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302445.8:c.433T= MANE Select ENSP00000303043.3:p.Tyr145=
ENST00000302445.7:c.433T= ENSP00000303043.3:p.Tyr145=
ENST00000319410.9:c.517T= ENSP00000325448.5:p.Tyr173=
ENST00000562875.5:c.223-405T= ENSP00000456185.1:n.223-405T=
ENST00000564578.5:c.351T= ENSP00000455818.1:p.Ser117=
ENST00000566249.5:c.235T=
ENST00000566560.5:n.547T=
ENST00000568378.5:c.146+7780T= ENSP00000454512.1:n.146+7780T=
ENST00000568682.5:c.-36T= ENSP00000462057.1:n.-36T=
ENST00000570215.1:c.517T= ENSP00000458028.1:p.Tyr173=
NM_001130089.1:c.517T= , LRG_366t1:c.517T= NP_001123561.1:p.Tyr173=
NM_005548.2:c.433T= NP_005539.1:p.Tyr145=
XM_017023217.1:c.-36T= XP_016878706.1:n.-36T=
NM_001130089.2:c.517T= NP_001123561.1:p.Tyr173=
NM_001378148.1:c.-36T= NP_001365077.1:n.-36T=
NM_005548.3:c.433T= MANE Select NP_005539.1:p.Tyr145=