Canonical Allele Identifier: CA1624927369

Gene: AARS2 TMEM151B POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44305004_44305005delinsAG , CM000668.2:g.44305004_44305005delinsAG	GRCh38
NC_000006.11:g.44272741_44272742delinsAG , CM000668.1:g.44272741_44272742delinsAG	GRCh37
NC_000006.10:g.44380719_44380720delinsAG	NCBI36
NG_031952.1:g.13322_13323delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.1579+49_1579+50delinsCT (AARS2) MANE Select	ENSP00000244571.4:n.1579+49_1579+50delinsCT
ENST00000244571.4:c.1579+49_1579+50delinsCT (AARS2)	ENSP00000244571.4:n.1579+49_1579+50delinsCT
ENST00000438774.2:c.577-1939_577-1938delinsAG (TMEM151B)	ENSP00000409337.2:n.577-1939_577-1938delinsAG
ENST00000505802.1:c.314-1939_314-1938delinsAG
NM_020745.3:c.1579+49_1579+50delinsCT (AARS2)	NP_065796.1:n.1579+49_1579+50delinsCT
XM_005249245.2:c.1288+49_1288+50delinsCT (AARS2)	XP_005249302.1:n.1288+49_1288+50delinsCT
XM_011514764.1:c.1579+49_1579+50delinsCT (AARS2)	XP_011513066.1:n.1579+49_1579+50delinsCT
XR_241907.2:n.1614+49_1614+50delinsCT (AARS2)
XM_005249245.3:c.1288+49_1288+50delinsCT (AARS2)	XP_005249302.1:n.1288+49_1288+50delinsCT
XM_011514764.2:c.1579+49_1579+50delinsCT (AARS2)	XP_011513066.1:n.1579+49_1579+50delinsCT
XM_017011112.1:c.289+49_289+50delinsCT (AARS2)	XP_016866601.1:n.289+49_289+50delinsCT
NM_020745.4:c.1579+49_1579+50delinsCT (AARS2) MANE Select	NP_065796.2:n.1579+49_1579+50delinsCT
NM_001318876.2:c.946-136886_946-136885delinsAG (POLR1C)	NP_001305805.1:n.946-136886_946-136885delinsAG