Canonical Allele Identifier: CA2648643618
Gene: ATP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160139530_160139539del , CM000663.2:g.160139530_160139539del GRCh38
NC_000001.10:g.160109320_160109329del , CM000663.1:g.160109320_160109329del GRCh37
NC_000001.9:g.158375944_158375953del NCBI36
NG_008014.1:g.28773_28782del , LRG_6:g.28773_28782del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.2841-110_2841-101del MANE Select ENSP00000354490.3:n.2841-110_2841-101del
ENST00000361216.7:c.2841-110_2841-101del ENSP00000354490.3:n.2841-110_2841-101del
ENST00000392233.7:c.2841-110_2841-101del ENSP00000376066.3:n.2841-110_2841-101del
ENST00000447527.1:c.1922-110_1922-101del
ENST00000463989.1:n.177-110_177-101del
NM_000702.3:c.2841-110_2841-101del NP_000693.1:n.2841-110_2841-101del
NM_000702.4:c.2841-110_2841-101del MANE Select NP_000693.1:n.2841-110_2841-101del