Canonical Allele Identifier: CA1624922781

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44302009T= , CM000668.2:g.44302009T= GRCh38
NC_000006.11:g.44269746T= , CM000668.1:g.44269746T= GRCh37
NC_000006.10:g.44377724T= NCBI36
NG_031952.1:g.16318A=

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.2598+51A= (AARS2) MANE Select ENSP00000244571.4:n.2598+51A=
ENST00000244571.4:c.2598+51A= (AARS2) ENSP00000244571.4:n.2598+51A=
ENST00000438774.2:c.577-4934T= (TMEM151B) ENSP00000409337.2:n.577-4934T=
ENST00000505802.1:c.314-4934T=
NM_020745.3:c.2598+51A= (AARS2) NP_065796.1:n.2598+51A=
XM_005249245.2:c.2307+51A= (AARS2) XP_005249302.1:n.2307+51A=
XM_011514764.1:c.2598+51A= (AARS2) XP_011513066.1:n.2598+51A=
XR_241907.2:n.2523+51A= (AARS2)
XM_005249245.3:c.2307+51A= (AARS2) XP_005249302.1:n.2307+51A=
XM_011514764.2:c.2598+51A= (AARS2) XP_011513066.1:n.2598+51A=
XM_017011112.1:c.1308+51A= (AARS2) XP_016866601.1:n.1308+51A=
NM_020745.4:c.2598+51A= (AARS2) MANE Select NP_065796.2:n.2598+51A=
NM_001318876.2:c.946-139881T= (POLR1C) NP_001305805.1:n.946-139881T=