Canonical Allele Identifier: CA1339676304

Gene: BOK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241563541C= , CM000664.2:g.241563541C=	GRCh38
NC_000002.11:g.242502956C= , CM000664.1:g.242502956C=	GRCh37
NC_000002.10:g.242151629C=	NCBI36
NG_029488.1:g.9765C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318407.5:c.349+1065C= MANE Select	ENSP00000314132.3:n.349+1065C=
ENST00000318407.4:c.349+1065C=	ENSP00000314132.3:n.349+1065C=
NM_032515.4:c.349+1065C=	NP_115904.1:n.349+1065C=
XM_005247037.3:c.349+1065C=	XP_005247094.1:n.349+1065C=
XM_005247039.3:c.115+1065C=	XP_005247096.1:n.115+1065C=
XM_011511696.1:c.349+1065C=	XP_011509998.1:n.349+1065C=
XM_011511697.1:c.349+1065C=	XP_011509999.1:n.349+1065C=
XM_011511696.2:c.349+1065C=	XP_011509998.1:n.349+1065C=
XM_011511697.3:c.349+1065C=	XP_011509999.1:n.349+1065C=
XM_017004775.1:c.115+1065C=	XP_016860264.1:n.115+1065C=
XM_017004776.1:c.115+1065C=	XP_016860265.1:n.115+1065C=
NM_032515.5:c.349+1065C= MANE Select	NP_115904.1:n.349+1065C=