Canonical Allele Identifier: CA1586866275

Gene: HARS2

Linked Data

• dbSNP Id: rs1759703258

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140695481_140695490del , CM000667.2:g.140695481_140695490del	GRCh38
NC_000005.9:g.140075066_140075075del , CM000667.1:g.140075066_140075075del	GRCh37
NC_000005.8:g.140055250_140055259del	NCBI36
NG_021415.1:g.9049_9058del
NG_032158.1:g.898_907del

Transcript Alleles

HGVS	Amino-acid change
ENST00000230771.9:c.400-27_400-18del MANE Select	ENSP00000230771.3:n.400-27_400-18del
ENST00000503873.6:c.304-257_304-248del	ENSP00000424516.2:n.304-257_304-248del
ENST00000509299.6:c.190-27_190-18del	ENSP00000425695.2:n.190-27_190-18del
ENST00000520095.6:c.*104-257_*104-248del	ENSP00000429220.1:n.*104-257_*104-248del
ENST00000642452.1:c.366-27_366-18del
ENST00000642752.1:c.400-27_400-18del	ENSP00000493630.1:n.400-27_400-18del
ENST00000642970.1:c.190-27_190-18del	ENSP00000496011.1:n.190-27_190-18del
ENST00000643996.1:c.190-27_190-18del	ENSP00000495350.1:n.190-27_190-18del
ENST00000645065.1:c.418-27_418-18del	ENSP00000493571.1:n.418-27_418-18del
ENST00000645749.1:c.400-27_400-18del	ENSP00000494296.1:n.400-27_400-18del
ENST00000646468.1:c.418-27_418-18del	ENSP00000494965.1:n.418-27_418-18del
ENST00000647484.1:c.190-27_190-18del	ENSP00000494140.1:n.190-27_190-18del
ENST00000230771.7:c.400-27_400-18del	ENSP00000230771.3:n.400-27_400-18del
ENST00000448069.2:c.109-257_109-248del	ENSP00000407105.2:n.109-257_109-248del
ENST00000502303.5:n.483-27_483-18del
ENST00000508522.5:c.325-27_325-18del	ENSP00000423616.1:n.325-27_325-18del
ENST00000509299.5:c.418-27_418-18del	ENSP00000425695.1:n.418-27_418-18del
ENST00000510104.5:c.*200-27_*200-18del	ENSP00000423530.1:n.*200-27_*200-18del
ENST00000513688.1:n.407-27_407-18del
ENST00000520095.5:c.*104-257_*104-248del	ENSP00000429220.1:n.*104-257_*104-248del
NM_001278731.1:c.325-27_325-18del	NP_001265660.1:n.325-27_325-18del
NM_001278732.1:c.94-257_94-248del	NP_001265661.1:n.94-257_94-248del
NM_012208.3:c.400-27_400-18del	NP_036340.1:n.400-27_400-18del
XM_011537619.1:c.418-27_418-18del	XP_011535921.1:n.418-27_418-18del
XM_011537620.1:c.418-27_418-18del	XP_011535922.1:n.418-27_418-18del
NM_001363535.1:c.418-27_418-18del	NP_001350464.1:n.418-27_418-18del
NM_001363536.1:c.190-27_190-18del	NP_001350465.1:n.190-27_190-18del
XM_017009288.1:c.190-27_190-18del	XP_016864777.1:n.190-27_190-18del
XM_017009289.1:c.190-27_190-18del	XP_016864778.1:n.190-27_190-18del
XM_017009290.2:c.-335-27_-335-18del	XP_016864779.1:n.-335-27_-335-18del
XM_017009291.1:c.-335-27_-335-18del	XP_016864780.1:n.-335-27_-335-18del
XM_017009292.1:c.-335-27_-335-18del	XP_016864781.1:n.-335-27_-335-18del
NM_012208.4:c.400-27_400-18del MANE Select	NP_036340.1:n.400-27_400-18del
NM_001278731.2:c.325-27_325-18del	NP_001265660.1:n.325-27_325-18del
NM_001278732.2:c.94-257_94-248del	NP_001265661.1:n.94-257_94-248del
NM_001363535.2:c.418-27_418-18del	NP_001350464.1:n.418-27_418-18del
NM_001363536.2:c.190-27_190-18del	NP_001350465.1:n.190-27_190-18del