Canonical Allele Identifier: CA2018023588

Gene: ATP11A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.112882313A= , CM000675.2:g.112882313A=	GRCh38
NC_000013.10:g.113536627A= , CM000675.1:g.113536627A=	GRCh37
NC_000013.9:g.112584628A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015205.3:c.*447A= MANE Select	NP_056020.2:n.*447A=
ENST00000375645.8:c.*447A= MANE Select	ENSP00000364796.3:n.*447A=
NM_015205.2:c.*447A=	NP_056020.2:n.*447A=
NM_032189.3:c.*249A=	NP_115565.3:n.*249A=
NM_032189.4:c.*249A=	NP_115565.3:n.*249A=
ENST00000375630.6:c.*249A=	ENSP00000364781.2:n.*249A=
ENST00000375645.7:c.*447A=	ENSP00000364796.3:n.*447A=
ENST00000419631.1:c.801A=	ENSP00000410824.1:n.801A=
ENST00000471555.5:c.1986A=
ENST00000487903.5:c.*510A=	ENSP00000420387.1:n.*510A=
ENST00000614170.1:n.1342A=
XM_005268299.3:c.*249A=	XP_005268356.1:n.*249A=
XM_005268299.4:c.*249A=	XP_005268356.1:n.*249A=
XM_005268300.3:c.*249A=	XP_005268357.1:n.*249A=
XM_005268300.4:c.*249A=	XP_005268357.1:n.*249A=
XM_005268305.3:c.*510A=	XP_005268362.1:n.*510A=
XM_005268305.4:c.*510A=	XP_005268362.1:n.*510A=
XM_005268306.4:c.*507A=	XP_005268363.1:n.*507A=
XM_011537478.1:c.*249A=	XP_011535780.1:n.*249A=
XM_011537479.1:c.*249A=	XP_011535781.1:n.*249A=
XM_011537481.1:c.*249A=	XP_011535783.1:n.*249A=