Canonical Allele Identifier: CA1854266876

Gene: APBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69488398G= , CM000671.2:g.69488398G=	GRCh38
NC_000009.11:g.72103314G= , CM000671.1:g.72103314G=	GRCh37
NC_000009.10:g.71293134G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001163.4:c.1201-12255C= MANE Select	NP_001154.2:n.1201-12255C=
ENST00000265381.7:c.1201-12255C= MANE Select	ENSP00000265381.3:n.1201-12255C=
NM_001163.3:c.1201-12255C=	NP_001154.2:n.1201-12255C=
ENST00000265381.6:c.1201-12255C=	ENSP00000265381.3:n.1201-12255C=
ENST00000699288.1:c.45+6940C=	ENSP00000514269.1:n.45+6940C=
XM_005251968.2:c.1201-12255C=	XP_005252025.1:n.1201-12255C=
XM_005251968.3:c.1201-12255C=	XP_005252025.1:n.1201-12255C=
XM_006717093.2:c.1201-12255C=	XP_006717156.1:n.1201-12255C=
XM_011518617.1:c.1201-12255C=	XP_011516919.1:n.1201-12255C=
XM_011518617.2:c.1201-12255C=	XP_011516919.1:n.1201-12255C=
XM_017014670.1:c.1201-12255C=	XP_016870159.1:n.1201-12255C=