Canonical Allele Identifier: CA2213393507

Gene: EARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23535236C= , CM000678.2:g.23535236C=	GRCh38
NC_000016.9:g.23546557C= , CM000678.1:g.23546557C=	GRCh37
NC_000016.8:g.23454058C=	NCBI36
NG_027752.1:g.27140G=
NG_027752.2:g.27140G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449606.7:c.610G= MANE Select	ENSP00000395196.2:p.Gly204=
ENST00000674054.1:c.610G=	ENSP00000501251.1:p.Gly204=
ENST00000449606.5:c.610G=	ENSP00000395196.1:p.Gly204=
ENST00000562402.1:n.214G=
ENST00000563232.1:c.610G=	ENSP00000456218.1:p.Gly204=
ENST00000563459.5:c.610G=	ENSP00000456467.1:p.Gly204=
ENST00000564501.5:c.610G=	ENSP00000457107.1:p.Gly204=
ENST00000564987.1:n.234G=
NM_001083614.1:c.610G=	NP_001077083.1:p.Gly204=
NM_001308211.1:c.610G=	NP_001295140.1:p.Gly204=
NR_003501.1:n.642G=
XM_011545738.1:c.538G=	XP_011544040.1:p.Gly180=
XM_011545739.1:c.331G=	XP_011544041.1:p.Gly111=
XR_001751841.1:n.932G=
NM_001083614.2:c.610G= MANE Select	NP_001077083.1:p.Gly204=
NR_003501.2:n.617G=