Canonical Allele Identifier: CA131933162

Gene: RARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.168492466C>A , CM000667.2:g.168492466C>A	GRCh38
NC_000005.9:g.167919471C>A , CM000667.1:g.167919471C>A	GRCh37
NC_000005.8:g.167852049C>A	NCBI36
NG_041809.1:g.11009C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002887.4:c.181-193C>A MANE Select	NP_002878.2:n.181-193C>A
ENST00000231572.8:c.181-193C>A MANE Select	ENSP00000231572.3:n.181-193C>A
NM_002887.3:c.181-193C>A	NP_002878.2:n.181-193C>A
ENST00000231572.7:c.181-193C>A	ENSP00000231572.3:n.181-193C>A
ENST00000519346.1:n.46-193C>A
ENST00000520013.5:c.181-193C>A	ENSP00000429030.1:n.181-193C>A
ENST00000521329.5:c.*122-193C>A	ENSP00000428494.1:n.*122-193C>A
ENST00000521939.5:n.194-193C>A
ENST00000522834.5:c.181-193C>A	ENSP00000430035.1:n.181-193C>A
ENST00000524082.5:n.229-193C>A