Canonical Allele Identifier: CA357972650

Gene: AIMP1

Linked Data

• MyVariant Identifiers: chr4:g.107248633G>C (hg19) ; chr4:g.106327476G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.106327476G>C , CM000666.2:g.106327476G>C	GRCh38
NC_000004.11:g.107248633G>C , CM000666.1:g.107248633G>C	GRCh37
NC_000004.10:g.107468082G>C	NCBI36
NG_028166.1:g.16867G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394701.6:c.-136G>C	ENSP00000378191.5:n.-136G>C
ENST00000442366.6:c.135G>C	ENSP00000405248.2:p.Glu45Asp
ENST00000673381.2:n.1196G>C
ENST00000683179.1:n.560G>C
ENST00000684504.1:c.135G>C	ENSP00000507352.1:p.Glu45Asp
ENST00000394701.5:c.207G>C	ENSP00000378191.4:p.Glu69Asp
ENST00000671868.1:c.135G>C	ENSP00000499850.1:p.Glu45Asp
ENST00000671960.1:c.135G>C	ENSP00000500025.1:p.Glu45Asp
ENST00000672003.1:c.135G>C	ENSP00000500187.1:p.Glu45Asp
ENST00000672285.1:c.135G>C	ENSP00000500668.1:p.Glu45Asp
ENST00000672328.1:c.135G>C	ENSP00000500159.1:p.Glu45Asp
ENST00000672337.1:c.135G>C	ENSP00000499921.1:p.Glu45Asp
ENST00000672341.1:c.135G>C MANE Select	ENSP00000500620.1:p.Glu45Asp
ENST00000672911.1:c.135G>C	ENSP00000500170.1:p.Glu45Asp
ENST00000673018.1:c.135G>C	ENSP00000500732.1:p.Glu45Asp
ENST00000673123.1:c.135G>C	ENSP00000500794.1:p.Glu45Asp
ENST00000673381.1:n.1196G>C
ENST00000358008.7:c.135G>C	ENSP00000350699.3:p.Glu45Asp
ENST00000394701.4:c.207G>C	ENSP00000378191.4:p.Glu69Asp
ENST00000442366.5:c.135G>C	ENSP00000405248.1:p.Glu45Asp
ENST00000510207.5:c.135G>C	ENSP00000423681.1:p.Glu45Asp
NM_001142415.1:c.135G>C	NP_001135887.1:p.Glu45Asp
NM_001142416.1:c.207G>C	NP_001135888.1:p.Glu69Asp
NM_004757.3:c.135G>C	NP_004748.2:p.Glu45Asp
XM_017008835.2:c.135G>C	XP_016864324.1:p.Glu45Asp
XM_017008836.2:c.135G>C	XP_016864325.1:p.Glu45Asp
NM_001142416.2:c.135G>C MANE Select	NP_001135888.2:p.Glu45Asp
NM_001142415.2:c.135G>C	NP_001135887.1:p.Glu45Asp
NM_004757.4:c.135G>C	NP_004748.2:p.Glu45Asp