Canonical Allele Identifier: CA494460627

Gene: EARS2

Linked Data

• MyVariant Identifiers: chr16:g.23546378G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23535057G>A , CM000678.2:g.23535057G>A	GRCh38
NC_000016.9:g.23546378G>A , CM000678.1:g.23546378G>A	GRCh37
NC_000016.8:g.23453879G>A	NCBI36
NG_027752.1:g.27319C>T
NG_027752.2:g.27319C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000449606.7:c.789C>T MANE Select	ENSP00000395196.2:p.Ala263=
ENST00000674054.1:c.789C>T	ENSP00000501251.1:p.Ala263=
ENST00000449606.5:c.789C>T	ENSP00000395196.1:p.Ala263=
ENST00000562402.1:n.393C>T
ENST00000563232.1:c.789C>T	ENSP00000456218.1:p.Ala263=
ENST00000563459.5:c.789C>T	ENSP00000456467.1:p.Ala263=
ENST00000564501.5:c.789C>T	ENSP00000457107.1:p.Ala263=
ENST00000564987.1:n.413C>T
ENST00000565344.1:n.162C>T
NM_001083614.1:c.789C>T	NP_001077083.1:p.Ala263=
NM_001308211.1:c.789C>T	NP_001295140.1:p.Ala263=
NR_003501.1:n.821C>T
XM_011545738.1:c.717C>T	XP_011544040.1:p.Ala239=
XM_011545739.1:c.510C>T	XP_011544041.1:p.Ala170=
XR_001751841.1:n.1111C>T
NM_001083614.2:c.789C>T MANE Select	NP_001077083.1:p.Ala263=
NR_003501.2:n.796C>T