Canonical Allele Identifier: CA2059865110

Gene: STAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.103745256C= , CM000674.2:g.103745256C=	GRCh38
NC_000012.11:g.104139034C= , CM000674.1:g.104139034C=	GRCh37
NC_000012.10:g.102663164C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388887.7:c.6115C= MANE Select	ENSP00000373539.2:p.Pro2039=
ENST00000388887.6:c.6115C=	ENSP00000373539.2:p.Pro2039=
NM_017564.9:c.6115C=	NP_060034.9:p.Pro2039=
XM_011538537.1:c.6115C=	XP_011536839.1:p.Pro2039=
XM_011538538.1:c.6115C=	XP_011536840.1:p.Pro2039=
XM_011538539.1:c.4444C=	XP_011536841.1:p.Pro1482=
XM_011538541.1:c.3514C=	XP_011536843.1:p.Pro1172=
XM_011538542.1:c.2176C=	XP_011536844.1:p.Pro726=
XR_429107.2:n.6335C=
XR_944609.1:n.6335C=
XM_011538537.2:c.6115C=	XP_011536839.1:p.Pro2039=
XM_011538538.3:c.6115C=	XP_011536840.1:p.Pro2039=
XM_011538539.2:c.4444C=	XP_011536841.1:p.Pro1482=
XM_011538541.2:c.3514C=	XP_011536843.1:p.Pro1172=
XM_011538542.2:c.2176C=	XP_011536844.1:p.Pro726=
XM_017019585.1:c.6115C=	XP_016875074.1:p.Pro2039=
XR_429107.3:n.6342C=
NM_017564.10:c.6115C= MANE Select	NP_060034.9:p.Pro2039=