Canonical Allele Identifier: CA131930287
Gene: RARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.168488351C>T , CM000667.2:g.168488351C>T GRCh38
NC_000005.9:g.167915356C>T , CM000667.1:g.167915356C>T GRCh37
NC_000005.8:g.167847934C>T NCBI36
NG_041809.1:g.6894C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231572.8:c.46-251C>T MANE Select ENSP00000231572.3:n.46-251C>T
ENST00000231572.7:c.46-251C>T ENSP00000231572.3:n.46-251C>T
ENST00000520013.5:c.46-251C>T ENSP00000429030.1:n.46-251C>T
ENST00000521329.5:c.163+81C>T ENSP00000428494.1:n.163+81C>T
ENST00000521939.5:n.59-251C>T
ENST00000522834.5:c.46-251C>T ENSP00000430035.1:n.46-251C>T
ENST00000524082.5:n.94-251C>T
ENST00000626454.1:c.163+81C>T ENSP00000486284.1:n.163+81C>T
NM_002887.3:c.46-251C>T NP_002878.2:n.46-251C>T
NM_002887.4:c.46-251C>T MANE Select NP_002878.2:n.46-251C>T