Canonical Allele Identifier: CA1483160096

Gene: AIMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.106327487G= , CM000666.2:g.106327487G=	GRCh38
NC_000004.11:g.107248644G= , CM000666.1:g.107248644G=	GRCh37
NC_000004.10:g.107468093G=	NCBI36
NG_028166.1:g.16878G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394701.6:c.-125G=	ENSP00000378191.5:n.-125G=
ENST00000442366.6:c.146G=	ENSP00000405248.2:p.Arg49=
ENST00000673381.2:n.1207G=
ENST00000683179.1:n.571G=
ENST00000684504.1:c.146G=	ENSP00000507352.1:p.Arg49=
ENST00000394701.5:c.218G=	ENSP00000378191.4:p.Arg73=
ENST00000671868.1:c.146G=	ENSP00000499850.1:p.Arg49=
ENST00000671960.1:c.146G=	ENSP00000500025.1:p.Arg49=
ENST00000672003.1:c.146G=	ENSP00000500187.1:p.Arg49=
ENST00000672285.1:c.146G=	ENSP00000500668.1:p.Arg49=
ENST00000672328.1:c.146G=	ENSP00000500159.1:p.Arg49=
ENST00000672337.1:c.146G=	ENSP00000499921.1:p.Arg49=
ENST00000672341.1:c.146G= MANE Select	ENSP00000500620.1:p.Arg49=
ENST00000672911.1:c.146G=	ENSP00000500170.1:p.Arg49=
ENST00000673018.1:c.146G=	ENSP00000500732.1:p.Arg49=
ENST00000673123.1:c.146G=	ENSP00000500794.1:p.Arg49=
ENST00000673381.1:n.1207G=
ENST00000358008.7:c.146G=	ENSP00000350699.3:p.Arg49=
ENST00000394701.4:c.218G=	ENSP00000378191.4:p.Arg73=
ENST00000442366.5:c.146G=	ENSP00000405248.1:p.Arg49=
ENST00000510207.5:c.146G=	ENSP00000423681.1:p.Arg49=
NM_001142415.1:c.146G=	NP_001135887.1:p.Arg49=
NM_001142416.1:c.218G=	NP_001135888.1:p.Arg73=
NM_004757.3:c.146G=	NP_004748.2:p.Arg49=
XM_017008835.2:c.146G=	XP_016864324.1:p.Arg49=
XM_017008836.2:c.146G=	XP_016864325.1:p.Arg49=
NM_001142416.2:c.146G= MANE Select	NP_001135888.2:p.Arg49=
NM_001142415.2:c.146G=	NP_001135887.1:p.Arg49=
NM_004757.4:c.146G=	NP_004748.2:p.Arg49=