Canonical Allele Identifier: CA494460591

Gene: EARS2

Linked Data

• MyVariant Identifiers: chr16:g.23546363T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23535042T>C , CM000678.2:g.23535042T>C	GRCh38
NC_000016.9:g.23546363T>C , CM000678.1:g.23546363T>C	GRCh37
NC_000016.8:g.23453864T>C	NCBI36
NG_027752.1:g.27334A>G
NG_027752.2:g.27334A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449606.7:c.804A>G MANE Select	ENSP00000395196.2:p.Pro268=
ENST00000674054.1:c.804A>G	ENSP00000501251.1:p.Pro268=
ENST00000449606.5:c.804A>G	ENSP00000395196.1:p.Pro268=
ENST00000562402.1:n.408A>G
ENST00000563232.1:c.804A>G	ENSP00000456218.1:p.Pro268=
ENST00000563459.5:c.804A>G	ENSP00000456467.1:p.Pro268=
ENST00000564501.5:c.804A>G	ENSP00000457107.1:p.Pro268=
ENST00000564987.1:n.428A>G
ENST00000565344.1:n.177A>G
NM_001083614.1:c.804A>G	NP_001077083.1:p.Pro268=
NM_001308211.1:c.804A>G	NP_001295140.1:p.Pro268=
NR_003501.1:n.836A>G
XM_011545738.1:c.732A>G	XP_011544040.1:p.Pro244=
XM_011545739.1:c.525A>G	XP_011544041.1:p.Pro175=
XR_001751841.1:n.1126A>G
NM_001083614.2:c.804A>G MANE Select	NP_001077083.1:p.Pro268=
NR_003501.2:n.811A>G