Canonical Allele Identifier: CA1624928866
Gene: AARS2 HGNC NCBI
POLR1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44311142G= , CM000668.2:g.44311142G= GRCh38
NC_000006.11:g.44278879G= , CM000668.1:g.44278879G= GRCh37
NC_000006.10:g.44386857G= NCBI36
NG_031952.1:g.7185C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.601C= (AARS2) MANE Select ENSP00000244571.4:p.Leu201=
ENST00000244571.4:c.601C= (AARS2) ENSP00000244571.4:p.Leu201=
ENST00000505802.1:c.855+3500G=
NM_020745.3:c.601C= (AARS2) NP_065796.1:p.Leu201=
XM_005249245.2:c.601C= (AARS2) XP_005249302.1:p.Leu201=
XM_011514764.1:c.601C= (AARS2) XP_011513066.1:p.Leu201=
XR_241907.2:n.636C= (AARS2)
XM_005249245.3:c.601C= (AARS2) XP_005249302.1:p.Leu201=
XM_011514764.2:c.601C= (AARS2) XP_011513066.1:p.Leu201=
XM_017011112.1:c.-418C= (AARS2) XP_016866601.1:n.-418C=
NM_020745.4:c.601C= (AARS2) MANE Select NP_065796.2:p.Leu201=
NM_001318876.2:c.946-130748G= (POLR1C) NP_001305805.1:n.946-130748G=