Canonical Allele Identifier: CA1624922581

Gene: AARS2 TMEM151B POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44301798_44301799delinsAG , CM000668.2:g.44301798_44301799delinsAG	GRCh38
NC_000006.11:g.44269535_44269536delinsAG , CM000668.1:g.44269535_44269536delinsAG	GRCh37
NC_000006.10:g.44377513_44377514delinsAG	NCBI36
NG_031952.1:g.16528_16529delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.2598+261_2598+262delinsCT (AARS2) MANE Select	ENSP00000244571.4:n.2598+261_2598+262delinsCT
ENST00000244571.4:c.2598+261_2598+262delinsCT (AARS2)	ENSP00000244571.4:n.2598+261_2598+262delinsCT
ENST00000438774.2:c.577-5145_577-5144delinsAG (TMEM151B)	ENSP00000409337.2:n.577-5145_577-5144delinsAG
ENST00000505802.1:c.314-5145_314-5144delinsAG
NM_020745.3:c.2598+261_2598+262delinsCT (AARS2)	NP_065796.1:n.2598+261_2598+262delinsCT
XM_005249245.2:c.2307+261_2307+262delinsCT (AARS2)	XP_005249302.1:n.2307+261_2307+262delinsCT
XM_011514764.1:c.2598+261_2598+262delinsCT (AARS2)	XP_011513066.1:n.2598+261_2598+262delinsCT
XR_241907.2:n.2523+261_2523+262delinsCT (AARS2)
XM_005249245.3:c.2307+261_2307+262delinsCT (AARS2)	XP_005249302.1:n.2307+261_2307+262delinsCT
XM_011514764.2:c.2598+261_2598+262delinsCT (AARS2)	XP_011513066.1:n.2598+261_2598+262delinsCT
XM_017011112.1:c.1308+261_1308+262delinsCT (AARS2)	XP_016866601.1:n.1308+261_1308+262delinsCT
NM_020745.4:c.2598+261_2598+262delinsCT (AARS2) MANE Select	NP_065796.2:n.2598+261_2598+262delinsCT
NM_001318876.2:c.946-140092_946-140091delinsAG (POLR1C)	NP_001305805.1:n.946-140092_946-140091delinsAG