Canonical Allele Identifier: CA2671672094

Gene: AIMP1

Linked Data

• gnomAD v4: 4-106327362-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.106327362T>C , CM000666.2:g.106327362T>C	GRCh38
NC_000004.11:g.107248519T>C , CM000666.1:g.107248519T>C	GRCh37
NC_000004.10:g.107467968T>C	NCBI36
NG_028166.1:g.16753T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394701.6:c.-161-89T>C	ENSP00000378191.5:n.-161-89T>C
ENST00000442366.6:c.110-89T>C	ENSP00000405248.2:n.110-89T>C
ENST00000673381.2:n.1171-89T>C
ENST00000683179.1:n.535-89T>C
ENST00000684504.1:c.110-89T>C	ENSP00000507352.1:n.110-89T>C
ENST00000394701.5:c.182-89T>C	ENSP00000378191.4:n.182-89T>C
ENST00000671868.1:c.110-89T>C	ENSP00000499850.1:n.110-89T>C
ENST00000671960.1:c.110-89T>C	ENSP00000500025.1:n.110-89T>C
ENST00000672003.1:c.110-89T>C	ENSP00000500187.1:n.110-89T>C
ENST00000672285.1:c.110-89T>C	ENSP00000500668.1:n.110-89T>C
ENST00000672328.1:c.110-89T>C	ENSP00000500159.1:n.110-89T>C
ENST00000672337.1:c.110-89T>C	ENSP00000499921.1:n.110-89T>C
ENST00000672341.1:c.110-89T>C MANE Select	ENSP00000500620.1:n.110-89T>C
ENST00000672911.1:c.110-89T>C	ENSP00000500170.1:n.110-89T>C
ENST00000673018.1:c.110-89T>C	ENSP00000500732.1:n.110-89T>C
ENST00000673123.1:c.110-89T>C	ENSP00000500794.1:n.110-89T>C
ENST00000673381.1:n.1171-89T>C
ENST00000358008.7:c.110-89T>C	ENSP00000350699.3:n.110-89T>C
ENST00000394701.4:c.182-89T>C	ENSP00000378191.4:n.182-89T>C
ENST00000442366.5:c.110-89T>C	ENSP00000405248.1:n.110-89T>C
ENST00000510207.5:c.110-89T>C	ENSP00000423681.1:n.110-89T>C
NM_001142415.1:c.110-89T>C	NP_001135887.1:n.110-89T>C
NM_001142416.1:c.182-89T>C	NP_001135888.1:n.182-89T>C
NM_004757.3:c.110-89T>C	NP_004748.2:n.110-89T>C
XM_017008835.2:c.110-89T>C	XP_016864324.1:n.110-89T>C
XM_017008836.2:c.110-89T>C	XP_016864325.1:n.110-89T>C
NM_001142416.2:c.110-89T>C MANE Select	NP_001135888.2:n.110-89T>C
NM_001142415.2:c.110-89T>C	NP_001135887.1:n.110-89T>C
NM_004757.4:c.110-89T>C	NP_004748.2:n.110-89T>C