Canonical Allele Identifier: CA396814402
Gene: KARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.75636512G>T , CM000678.2:g.75636512G>T GRCh38
NC_000016.9:g.75670410G>T , CM000678.1:g.75670410G>T GRCh37
NC_000016.8:g.74227911G>T NCBI36
NG_028025.1:g.16176C>A , LRG_366:g.16176C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302445.8:c.424C>A MANE Select ENSP00000303043.3:p.Leu142Ile
ENST00000302445.7:c.424C>A ENSP00000303043.3:p.Leu142Ile
ENST00000319410.9:c.508C>A ENSP00000325448.5:p.Leu170Ile
ENST00000562875.5:c.223-414C>A ENSP00000456185.1:n.223-414C>A
ENST00000564578.5:c.342C>A ENSP00000455818.1:p.Ser114Arg
ENST00000566249.5:c.226C>A
ENST00000566560.5:n.538C>A
ENST00000568378.5:c.146+7771C>A ENSP00000454512.1:n.146+7771C>A
ENST00000568682.5:c.-45C>A ENSP00000462057.1:n.-45C>A
ENST00000570215.1:c.508C>A ENSP00000458028.1:p.Leu170Ile
NM_001130089.1:c.508C>A , LRG_366t1:c.508C>A NP_001123561.1:p.Leu170Ile
NM_005548.2:c.424C>A NP_005539.1:p.Leu142Ile
XM_017023217.1:c.-45C>A XP_016878706.1:n.-45C>A
NM_001130089.2:c.508C>A NP_001123561.1:p.Leu170Ile
NM_001378148.1:c.-45C>A NP_001365077.1:n.-45C>A
NM_005548.3:c.424C>A MANE Select NP_005539.1:p.Leu142Ile