Canonical Allele Identifier: CA612642639

Gene: CARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110687840G>C , CM000675.2:g.110687840G>C	GRCh38
NC_000013.10:g.111340187G>C , CM000675.1:g.111340187G>C	GRCh37
NC_000013.9:g.110138188G>C	NCBI36
NG_042045.1:g.23341C>G
NG_042045.2:g.30762C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024537.4:c.466-14C>G MANE Select	NP_078813.1:n.466-14C>G
ENST00000257347.9:c.466-14C>G MANE Select	ENSP00000257347.4:n.466-14C>G
NM_001352252.1:c.-534-14C>G	NP_001339181.1:n.-534-14C>G
NM_001352252.2:c.-534-14C>G	NP_001339181.1:n.-534-14C>G
NM_001352253.1:c.466-14C>G	NP_001339182.1:n.466-14C>G
NM_001352253.2:c.466-14C>G	NP_001339182.1:n.466-14C>G
NM_001352253.3:c.466-14C>G	NP_001339182.1:n.466-14C>G
NM_024537.2:c.466-14C>G	NP_078813.1:n.466-14C>G
NM_024537.3:c.466-14C>G	NP_078813.1:n.466-14C>G
NR_147941.1:n.437-14C>G
NR_147942.1:n.553-14C>G
NR_147942.2:n.489-14C>G
ENST00000257347.8:c.466-14C>G	ENSP00000257347.4:n.466-14C>G
ENST00000465145.5:n.391-14C>G
ENST00000535398.5:n.658-14C>G
ENST00000537394.5:c.*121-14C>G	ENSP00000437962.1:n.*121-14C>G
ENST00000539269.5:c.476-14C>G
ENST00000540629.5:n.497-14C>G
ENST00000541443.5:n.377-14C>G
ENST00000542126.5:n.462-14C>G
ENST00000542709.5:c.439-14C>G	ENSP00000444655.1:n.439-14C>G
ENST00000544488.5:n.387-4706C>G
XM_006719953.2:c.127-14C>G	XP_006720016.1:n.127-14C>G
XM_006719953.3:c.127-14C>G	XP_006720016.1:n.127-14C>G
XM_011521114.1:c.466-14C>G	XP_011519416.1:n.466-14C>G
XM_011521115.1:c.127-14C>G	XP_011519417.1:n.127-14C>G
XM_011521116.1:c.121-14C>G	XP_011519418.1:n.121-14C>G
XM_011521117.1:c.466-14C>G	XP_011519419.1:n.466-14C>G
XM_011521117.3:c.466-14C>G	XP_011519419.1:n.466-14C>G
XM_011521118.1:c.466-14C>G	XP_011519420.1:n.466-14C>G
XM_011521118.3:c.466-14C>G	XP_011519420.1:n.466-14C>G
XM_011521119.1:c.466-14C>G	XP_011519421.1:n.466-14C>G
XM_011521120.1:c.-215-4706C>G	XP_011519422.1:n.-215-4706C>G
XM_017020741.1:c.127-14C>G	XP_016876230.1:n.127-14C>G
XM_017020742.2:c.466-14C>G	XP_016876231.1:n.466-14C>G
XM_024449409.1:c.-215-4706C>G	XP_024305177.1:n.-215-4706C>G
XR_001749664.2:n.506-14C>G
XR_001749665.2:n.506-14C>G
XR_001749666.2:n.506-14C>G
XR_001749667.2:n.506-14C>G
XR_001749668.2:n.506-14C>G
XR_002957472.1:n.506-14C>G
XR_243047.2:n.489-14C>G
XR_243047.3:n.506-14C>G
XR_243048.3:n.489-14C>G
XR_243048.4:n.506-14C>G
XR_243049.3:n.489-14C>G
XR_243049.4:n.506-14C>G
XR_243051.2:n.489-14C>G
XR_243051.3:n.506-14C>G