Canonical Allele Identifier: CA1979846283

Gene: SPTBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66715958T= , CM000673.2:g.66715958T=	GRCh38
NC_000011.9:g.66483429T= , CM000673.1:g.66483429T=	GRCh37
NC_000011.8:g.66240005T=	NCBI36
NG_016150.1:g.10442A=
NG_016150.2:g.18404A=

Transcript Alleles

HGVS	Amino-acid Change
NM_006946.4:c.181A= MANE Select	NP_008877.2:p.Lys61=
ENST00000533211.6:c.181A= MANE Select	ENSP00000432568.1:p.Lys61=
NM_006946.2:c.181A=	NP_008877.1:p.Lys61=
NM_006946.3:c.181A=	NP_008877.1:p.Lys61=
ENST00000309996.6:c.181A=	ENSP00000311489.2:p.Lys61=
ENST00000309996.7:c.181A=	ENSP00000311489.2:p.Lys61=
ENST00000527010.1:c.181A=	ENSP00000433631.1:p.Lys61=
ENST00000529997.5:c.181A=	ENSP00000433593.1:p.Lys61=
ENST00000533211.5:c.181A=	ENSP00000432568.1:p.Lys61=
ENST00000611817.4:c.181A=	ENSP00000480692.1:p.Lys61=
ENST00000611817.5:c.181A=	ENSP00000480692.2:p.Lys61=
ENST00000617502.4:c.181A=	ENSP00000482000.1:p.Lys61=
ENST00000617502.5:c.202A=	ENSP00000482000.2:p.Lys68=
ENST00000647510.1:n.708A=
ENST00000647510.2:c.181A=	ENSP00000508362.1:p.Lys61=
ENST00000651232.1:c.202A=	ENSP00000499027.1:p.Lys68=
XM_005274192.3:c.181A=	XP_005274249.1:p.Lys61=
XM_005274192.4:c.181A=	XP_005274249.1:p.Lys61=
XM_005274193.3:c.181A=	XP_005274250.1:p.Lys61=
XM_006718669.2:c.202A=	XP_006718732.1:p.Lys68=
XM_006718669.3:c.202A=	XP_006718732.1:p.Lys68=
XM_006718671.2:c.181A=	XP_006718734.1:p.Lys61=
XM_006718671.4:c.181A=	XP_006718734.1:p.Lys61=
XM_011545216.1:c.202A=	XP_011543518.1:p.Lys68=
XM_011545216.3:c.202A=	XP_011543518.1:p.Lys68=
XM_011545217.1:c.202A=	XP_011543519.1:p.Lys68=
XM_011545217.2:c.202A=	XP_011543519.1:p.Lys68=
XM_017018174.1:c.181A=	XP_016873663.1:p.Lys61=
XM_017018175.2:c.181A=	XP_016873664.1:p.Lys61=
XM_017018176.1:c.181A=	XP_016873665.1:p.Lys61=
XM_017018177.2:c.181A=	XP_016873666.1:p.Lys61=
XM_017018178.1:c.181A=	XP_016873667.1:p.Lys61=