Canonical Allele Identifier: CA395133977

Gene: EARS2

Linked Data

• MyVariant Identifiers: chr16:g.23546478A>G (hg19) ; chr16:g.23535157A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23535157A>G , CM000678.2:g.23535157A>G	GRCh38
NC_000016.9:g.23546478A>G , CM000678.1:g.23546478A>G	GRCh37
NC_000016.8:g.23453979A>G	NCBI36
NG_027752.1:g.27219T>C
NG_027752.2:g.27219T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000449606.7:c.689T>C MANE Select	ENSP00000395196.2:p.Leu230Pro
ENST00000674054.1:c.689T>C	ENSP00000501251.1:p.Leu230Pro
ENST00000449606.5:c.689T>C	ENSP00000395196.1:p.Leu230Pro
ENST00000562402.1:n.293T>C
ENST00000563232.1:c.689T>C	ENSP00000456218.1:p.Leu230Pro
ENST00000563459.5:c.689T>C	ENSP00000456467.1:p.Leu230Pro
ENST00000564501.5:c.689T>C	ENSP00000457107.1:p.Leu230Pro
ENST00000564987.1:n.313T>C
ENST00000565344.1:n.62T>C
NM_001083614.1:c.689T>C	NP_001077083.1:p.Leu230Pro
NM_001308211.1:c.689T>C	NP_001295140.1:p.Leu230Pro
NR_003501.1:n.721T>C
XM_011545738.1:c.617T>C	XP_011544040.1:p.Leu206Pro
XM_011545739.1:c.410T>C	XP_011544041.1:p.Leu137Pro
XR_001751841.1:n.1011T>C
NM_001083614.2:c.689T>C MANE Select	NP_001077083.1:p.Leu230Pro
NR_003501.2:n.696T>C