Canonical Allele Identifier: CA2648643625
Gene: ATP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160139540_160139579dup , CM000663.2:g.160139540_160139579dup GRCh38
NC_000001.10:g.160109330_160109369dup , CM000663.1:g.160109330_160109369dup GRCh37
NC_000001.9:g.158375954_158375993dup NCBI36
NG_008014.1:g.28783_28822dup , LRG_6:g.28783_28822dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.2841-100_2841-61dup MANE Select ENSP00000354490.3:n.2841-100_2841-61dup
ENST00000361216.7:c.2841-100_2841-61dup ENSP00000354490.3:n.2841-100_2841-61dup
ENST00000392233.7:c.2841-100_2841-61dup ENSP00000376066.3:n.2841-100_2841-61dup
ENST00000447527.1:c.1922-100_1922-61dup
ENST00000463989.1:n.177-100_177-61dup
NM_000702.3:c.2841-100_2841-61dup NP_000693.1:n.2841-100_2841-61dup
NM_000702.4:c.2841-100_2841-61dup MANE Select NP_000693.1:n.2841-100_2841-61dup