Canonical Allele Identifier: CA494460637

Gene: EARS2

Linked Data

• MyVariant Identifiers: chr16:g.23546381C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23535060C>T , CM000678.2:g.23535060C>T	GRCh38
NC_000016.9:g.23546381C>T , CM000678.1:g.23546381C>T	GRCh37
NC_000016.8:g.23453882C>T	NCBI36
NG_027752.1:g.27316G>A
NG_027752.2:g.27316G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000449606.7:c.786G>A MANE Select	ENSP00000395196.2:p.Gln262=
ENST00000674054.1:c.786G>A	ENSP00000501251.1:p.Gln262=
ENST00000449606.5:c.786G>A	ENSP00000395196.1:p.Gln262=
ENST00000562402.1:n.390G>A
ENST00000563232.1:c.786G>A	ENSP00000456218.1:p.Gln262=
ENST00000563459.5:c.786G>A	ENSP00000456467.1:p.Gln262=
ENST00000564501.5:c.786G>A	ENSP00000457107.1:p.Gln262=
ENST00000564987.1:n.410G>A
ENST00000565344.1:n.159G>A
NM_001083614.1:c.786G>A	NP_001077083.1:p.Gln262=
NM_001308211.1:c.786G>A	NP_001295140.1:p.Gln262=
NR_003501.1:n.818G>A
XM_011545738.1:c.714G>A	XP_011544040.1:p.Gln238=
XM_011545739.1:c.507G>A	XP_011544041.1:p.Gln169=
XR_001751841.1:n.1108G>A
NM_001083614.2:c.786G>A MANE Select	NP_001077083.1:p.Gln262=
NR_003501.2:n.793G>A