Canonical Allele Identifier: CA1139879242

Gene: ATP2B4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.203682799T= , CM000663.2:g.203682799T=	GRCh38
NC_000001.10:g.203651927T= , CM000663.1:g.203651927T=	GRCh37
NC_000001.9:g.201918550T=	NCBI36
NG_029589.1:g.61013T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001684.5:c.-407T= MANE Select	NP_001675.3:n.-407T=
ENST00000357681.10:c.-407T= MANE Select	ENSP00000350310.5:n.-407T=
NM_001001396.2:c.-407T=	NP_001001396.1:n.-407T=
NM_001001396.3:c.-407T=	NP_001001396.1:n.-407T=
NM_001365783.1:c.-407T=	NP_001352712.1:n.-407T=
NM_001365783.2:c.-407T=	NP_001352712.1:n.-407T=
NM_001365784.1:c.-407T=	NP_001352713.1:n.-407T=
NM_001365784.2:c.-407T=	NP_001352713.1:n.-407T=
NM_001684.4:c.-407T=	NP_001675.3:n.-407T=
ENST00000341360.7:c.-407T=	ENSP00000340930.2:n.-407T=
ENST00000357681.9:c.-407T=	ENSP00000350310.5:n.-407T=
ENST00000367218.7:c.-407T=	ENSP00000356187.3:n.-407T=
ENST00000705901.1:c.-407T=	ENSP00000516177.1:n.-407T=