Canonical Allele Identifier: CA2084609691

Gene: SPART

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.36314260T= , CM000675.2:g.36314260T=	GRCh38
NC_000013.10:g.36888397T= , CM000675.1:g.36888397T=	GRCh37
NC_000013.9:g.35786397T=	NCBI36
NG_011559.1:g.60921A=
NG_011559.2:g.60921A=

Transcript Alleles

HGVS	Amino-acid Change
NM_015087.5:c.1450A= MANE Select	NP_055902.1:p.Thr484=
ENST00000438666.7:c.1450A= MANE Select	ENSP00000406061.2:p.Thr484=
NM_001142294.1:c.1450A=	NP_001135766.1:p.Thr484=
NM_001142294.2:c.1450A=	NP_001135766.1:p.Thr484=
NM_001142295.1:c.1450A=	NP_001135767.1:p.Thr484=
NM_001142295.2:c.1450A=	NP_001135767.1:p.Thr484=
NM_001142296.1:c.1450A=	NP_001135768.1:p.Thr484=
NM_001142296.2:c.1450A=	NP_001135768.1:p.Thr484=
NM_015087.4:c.1450A=	NP_055902.1:p.Thr484=
ENST00000355182.8:c.1450A=	ENSP00000347314.4:p.Thr484=
ENST00000438666.6:c.1450A=	ENSP00000406061.2:p.Thr484=
ENST00000451493.5:c.1450A=	ENSP00000414147.1:p.Thr484=
ENST00000475603.5:n.211A=
ENST00000482146.1:n.182A=
ENST00000494062.2:c.1450A=	ENSP00000473599.1:p.Thr484=
ENST00000650221.1:c.1450A=	ENSP00000497209.1:p.Thr484=
XM_005266313.3:c.1450A=	XP_005266370.1:p.Thr484=
XM_005266313.5:c.1450A=	XP_005266370.1:p.Thr484=
XM_005266314.2:c.1450A=	XP_005266371.1:p.Thr484=
XM_005266314.3:c.1450A=	XP_005266371.1:p.Thr484=
XM_005266315.2:c.1450A=	XP_005266372.1:p.Thr484=
XM_005266315.3:c.1450A=	XP_005266372.1:p.Thr484=
XM_005266316.2:c.1450A=	XP_005266373.1:p.Thr484=
XM_005266317.2:c.1450A=	XP_005266374.1:p.Thr484=
XM_005266317.3:c.1450A=	XP_005266374.1:p.Thr484=
XM_011535012.1:c.1450A=	XP_011533314.1:p.Thr484=
XM_011535012.2:c.1450A=	XP_011533314.1:p.Thr484=
XM_024449334.1:c.1450A=	XP_024305102.1:p.Thr484=
XR_001749523.2:n.1678A=
XR_941540.1:n.1712A=