Canonical Allele Identifier: CA406053175

Gene: ATP1A3

Linked Data

• MyVariant Identifiers: chr19:g.42489284A>G (hg19) ; chr19:g.41985132A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41985132A>G , CM000681.2:g.41985132A>G	GRCh38
NC_000019.9:g.42489284A>G , CM000681.1:g.42489284A>G	GRCh37
NC_000019.8:g.47181124A>G	NCBI36
NG_008015.1:g.14099T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.818T>C	ENSP00000444688.1:p.Ile273Thr
ENST00000644613.1:c.779T>C	ENSP00000494711.1:p.Ile260Thr
ENST00000648268.1:c.779T>C MANE Select	ENSP00000498113.1:p.Ile260Thr
ENST00000302102.9:c.779T>C	ENSP00000302397.5:p.Ile260Thr
ENST00000441343.5:c.779T>C	ENSP00000411503.1:p.Ile260Thr
ENST00000473086.3:c.689T>C	ENSP00000469129.2:p.Ile230Thr
ENST00000485672.2:n.92T>C
ENST00000543770.5:c.812T>C	ENSP00000437577.1:p.Ile271Thr
ENST00000545399.5:c.818T>C	ENSP00000444688.1:p.Ile273Thr
ENST00000602133.5:c.689T>C	ENSP00000471581.1:p.Ile230Thr
NM_001256213.1:c.812T>C	NP_001243142.1:p.Ile271Thr
NM_001256214.1:c.818T>C	NP_001243143.1:p.Ile273Thr
NM_152296.4:c.779T>C	NP_689509.1:p.Ile260Thr
XM_011526991.1:c.689T>C	XP_011525293.1:p.Ile230Thr
NM_152296.5:c.779T>C MANE Select	NP_689509.1:p.Ile260Thr
NM_001256214.2:c.818T>C	NP_001243143.1:p.Ile273Thr
NM_001256213.2:c.812T>C	NP_001243142.1:p.Ile271Thr