Canonical Allele Identifier: CA366745404

Gene: AIMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6009437A>G , CM000669.2:g.6009437A>G	GRCh38
NC_000007.13:g.6049068A>G , CM000669.1:g.6049068A>G	GRCh37
NC_000007.12:g.6015594A>G	NCBI36
NG_008466.1:g.4670T>C , LRG_161:g.4670T>C
NG_050738.1:g.5187A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006303.4:c.74A>G MANE Select	NP_006294.2:p.Tyr25Cys
ENST00000223029.8:c.74A>G MANE Select	ENSP00000223029.3:p.Tyr25Cys
NM_001326606.1:c.15+59A>G	NP_001313535.1:n.15+59A>G
NM_001326606.2:c.15+59A>G	NP_001313535.1:n.15+59A>G
NM_001326607.1:c.74A>G	NP_001313536.1:p.Tyr25Cys
NM_001326607.2:c.74A>G	NP_001313536.1:p.Tyr25Cys
NM_001326609.1:c.-247A>G	NP_001313538.1:n.-247A>G
NM_001326609.2:c.-247A>G	NP_001313538.1:n.-247A>G
NM_001326610.1:c.-251+59A>G	NP_001313539.1:n.-251+59A>G
NM_001326610.2:c.-251+59A>G	NP_001313539.1:n.-251+59A>G
NM_001326611.2:c.-238+59A>G	NP_001313540.1:n.-238+59A>G
NM_001326611.3:c.-238+59A>G	NP_001313540.1:n.-238+59A>G
NM_006303.3:c.74A>G	NP_006294.2:p.Tyr25Cys
ENST00000223029.7:c.74A>G	ENSP00000223029.3:p.Tyr25Cys
ENST00000395236.2:c.74A>G	ENSP00000378658.2:p.Tyr25Cys
ENST00000400479.6:c.-251+59A>G	ENSP00000383327.2:n.-251+59A>G
ENST00000415999.1:c.74A>G	ENSP00000392519.1:p.Tyr25Cys
XM_005249848.1:c.15+59A>G	XP_005249905.1:n.15+59A>G