Canonical Allele Identifier: CA1913151311

Gene: BICC1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.58795818A= , CM000672.2:g.58795818A=	GRCh38
NC_000010.10:g.60555578A= , CM000672.1:g.60555578A=	GRCh37
NC_000010.9:g.60225584A=	NCBI36
NG_029759.2:g.287675A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373886.8:c.1180-522A= MANE Select	ENSP00000362993.3:n.1180-522A=
ENST00000263103.1:c.58-522A=	ENSP00000263103.1:n.58-522A=
ENST00000373886.7:c.1180-522A=	ENSP00000362993.3:n.1180-522A=
NM_001080512.2:c.1180-522A=	NP_001073981.1:n.1180-522A=
XM_005270169.3:c.1039-522A=	XP_005270226.1:n.1039-522A=
XM_011540185.1:c.1252-522A=	XP_011538487.1:n.1252-522A=
XM_011540186.1:c.1252-522A=	XP_011538488.1:n.1252-522A=
XM_011540187.1:c.1252-522A=	XP_011538489.1:n.1252-522A=
XM_011540188.1:c.1036-522A=	XP_011538490.1:n.1036-522A=
XM_011540189.1:c.1024-522A=	XP_011538491.1:n.1024-522A=
XM_011540190.1:c.940-522A=	XP_011538492.1:n.940-522A=
XM_011540191.1:c.796-522A=	XP_011538493.1:n.796-522A=
XM_005270169.5:c.1039-522A=	XP_005270226.1:n.1039-522A=
XM_011540185.2:c.1252-522A=	XP_011538487.1:n.1252-522A=
XM_011540190.3:c.940-522A=	XP_011538492.1:n.940-522A=
XM_011540191.2:c.796-522A=	XP_011538493.1:n.796-522A=
XM_017016677.1:c.1048-522A=	XP_016872166.1:n.1048-522A=
XM_017016678.1:c.1036-522A=	XP_016872167.1:n.1036-522A=
XM_024448174.1:c.1267-522A=	XP_024303942.1:n.1267-522A=
XM_024448175.1:c.940-522A=	XP_024303943.1:n.940-522A=
NM_001080512.3:c.1180-522A= MANE Select	NP_001073981.1:n.1180-522A=