Canonical Allele Identifier: CA1979774444

Gene: SPTBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66694146T= , CM000673.2:g.66694146T=	GRCh38
NC_000011.9:g.66461617T= , CM000673.1:g.66461617T=	GRCh37
NC_000011.8:g.66218193T=	NCBI36
NG_016150.1:g.32254A=
NG_016150.2:g.40216A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309996.7:c.4496A=	ENSP00000311489.2:p.Asp1499=
ENST00000611817.5:c.4496A=	ENSP00000480692.2:p.Asp1499=
ENST00000617502.5:c.4517A=	ENSP00000482000.2:p.Asp1506=
ENST00000647510.2:c.4496A=	ENSP00000508362.1:p.Asp1499=
ENST00000533211.6:c.4496A= MANE Select	ENSP00000432568.1:p.Asp1499=
ENST00000647510.1:n.5023A=
ENST00000309996.6:c.4496A=	ENSP00000311489.2:p.Asp1499=
ENST00000529997.5:c.4496A=	ENSP00000433593.1:p.Asp1499=
ENST00000533211.5:c.4496A=	ENSP00000432568.1:p.Asp1499=
ENST00000611817.4:c.1855-5485A=	ENSP00000480692.1:n.1855-5485A=
ENST00000617502.4:c.1846-4790A=	ENSP00000482000.1:n.1846-4790A=
NM_006946.2:c.4496A=	NP_008877.1:p.Asp1499=
XM_005274192.3:c.4496A=	XP_005274249.1:p.Asp1499=
XM_005274193.3:c.4496A=	XP_005274250.1:p.Asp1499=
XM_006718669.2:c.4517A=	XP_006718732.1:p.Asp1506=
XM_006718671.2:c.4496A=	XP_006718734.1:p.Asp1499=
NM_006946.3:c.4496A=	NP_008877.1:p.Asp1499=
XM_005274192.4:c.4496A=	XP_005274249.1:p.Asp1499=
XM_006718669.3:c.4517A=	XP_006718732.1:p.Asp1506=
XM_006718671.4:c.4496A=	XP_006718734.1:p.Asp1499=
XM_017018174.1:c.4496A=	XP_016873663.1:p.Asp1499=
XM_017018175.2:c.4496A=	XP_016873664.1:p.Asp1499=
XM_017018176.1:c.4496A=	XP_016873665.1:p.Asp1499=
XM_017018177.2:c.4496A=	XP_016873666.1:p.Asp1499=
XM_017018178.1:c.4496A=	XP_016873667.1:p.Asp1499=
NM_006946.4:c.4496A= MANE Select	NP_008877.2:p.Asp1499=