Canonical Allele Identifier: CA15383854
Community Standard Title: NM_002887.4(RARS1):c.45+276G>A
Gene: RARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.168486819G>A , CM000667.2:g.168486819G>A GRCh38
NC_000005.9:g.167913824G>A , CM000667.1:g.167913824G>A GRCh37
NC_000005.8:g.167846402G>A NCBI36
NG_041809.1:g.5362G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002887.4:c.45+276G>A MANE Select NP_002878.2:n.45+276G>A
ENST00000231572.8:c.45+276G>A MANE Select ENSP00000231572.3:n.45+276G>A
NM_002887.3:c.45+276G>A NP_002878.2:n.45+276G>A
ENST00000231572.7:c.45+276G>A ENSP00000231572.3:n.45+276G>A
ENST00000520013.5:c.45+276G>A ENSP00000429030.1:n.45+276G>A
ENST00000521329.5:c.45+276G>A ENSP00000428494.1:n.45+276G>A
ENST00000521939.5:n.58+276G>A
ENST00000522834.5:c.45+276G>A ENSP00000430035.1:n.45+276G>A
ENST00000524082.5:n.93+276G>A
ENST00000626454.1:c.45+276G>A ENSP00000486284.1:n.45+276G>A