Canonical Allele Identifier: CA564065071
Community Standard Title: NM_002887.4(RARS1):c.46-16G>T
Gene: RARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.168488586G>T , CM000667.2:g.168488586G>T GRCh38
NC_000005.9:g.167915591G>T , CM000667.1:g.167915591G>T GRCh37
NC_000005.8:g.167848169G>T NCBI36
NG_041809.1:g.7129G>T

Transcript Alleles

HGVS Amino-acid Change
NM_002887.4:c.46-16G>T MANE Select NP_002878.2:n.46-16G>T
ENST00000231572.8:c.46-16G>T MANE Select ENSP00000231572.3:n.46-16G>T
NM_002887.3:c.46-16G>T NP_002878.2:n.46-16G>T
ENST00000231572.7:c.46-16G>T ENSP00000231572.3:n.46-16G>T
ENST00000520013.5:c.46-16G>T ENSP00000429030.1:n.46-16G>T
ENST00000521329.5:c.164-16G>T ENSP00000428494.1:n.164-16G>T
ENST00000521939.5:n.59-16G>T
ENST00000522834.5:c.46-16G>T ENSP00000430035.1:n.46-16G>T
ENST00000524082.5:n.94-16G>T
ENST00000626454.1:c.164-16G>T ENSP00000486284.1:n.164-16G>T