Canonical Allele Identifier: CA364335981

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44301382G>A , CM000668.2:g.44301382G>A GRCh38
NC_000006.11:g.44269119G>A , CM000668.1:g.44269119G>A GRCh37
NC_000006.10:g.44377097G>A NCBI36
NG_031952.1:g.16945C>T

Transcript Alleles

HGVS Amino-acid Change
NM_020745.4:c.2681C>T (AARS2) MANE Select NP_065796.2:p.Ser894Leu
ENST00000244571.5:c.2681C>T (AARS2) MANE Select ENSP00000244571.4:p.Ser894Leu
NM_001318876.2:c.946-140508G>A (POLR1C) NP_001305805.1:n.946-140508G>A
NM_020745.3:c.2681C>T (AARS2) NP_065796.1:p.Ser894Leu
ENST00000244571.4:c.2681C>T (AARS2) ENSP00000244571.4:p.Ser894Leu
ENST00000438774.2:c.577-5561G>A (TMEM151B) ENSP00000409337.2:n.577-5561G>A
ENST00000491573.1:n.39C>T (AARS2)
ENST00000505802.1:c.314-5561G>A
XM_005249245.2:c.2390C>T (AARS2) XP_005249302.1:p.Ser797Leu
XM_005249245.3:c.2390C>T (AARS2) XP_005249302.1:p.Ser797Leu
XM_011514764.1:c.2681C>T (AARS2) XP_011513066.1:p.Ser894Leu
XM_011514764.2:c.2681C>T (AARS2) XP_011513066.1:p.Ser894Leu
XM_017011112.1:c.1391C>T (AARS2) XP_016866601.1:p.Ser464Leu
XR_241907.2:n.2606C>T (AARS2)