Canonical Allele Identifier: CA10316928

Gene: SBF1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50460698G>A , CM000684.2:g.50460698G>A	GRCh38
NC_000022.10:g.50899127G>A , CM000684.1:g.50899127G>A	GRCh37
NC_000022.9:g.49245993G>A	NCBI36
NG_041810.1:g.19374C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.2982C>T	ENSP00000252027.8:p.Ala994=
ENST00000684986.1:c.2985C>T	ENSP00000509117.1:p.Ala995=
ENST00000685180.1:n.2324C>T
ENST00000685386.1:c.838-13C>T	ENSP00000510338.1:n.838-13C>T
ENST00000685390.1:n.1225C>T
ENST00000685809.1:c.2973C>T	ENSP00000508863.1:p.Ala991=
ENST00000686222.1:c.*2404C>T	ENSP00000508737.1:n.*2404C>T
ENST00000686427.1:c.2971C>T	ENSP00000510379.1:p.Leu991Phe
ENST00000686801.1:c.2970C>T	ENSP00000509915.1:p.Ala990=
ENST00000687016.1:c.2961C>T	ENSP00000509074.1:p.Ala987=
ENST00000687704.1:c.*796C>T	ENSP00000510454.1:n.*796C>T
ENST00000688030.1:c.791C>T	ENSP00000508668.1:n.791C>T
ENST00000688066.1:c.2982C>T	ENSP00000510782.1:p.Ala994=
ENST00000688124.1:c.*1976C>T	ENSP00000510645.1:n.*1976C>T
ENST00000688848.1:c.*2404C>T	ENSP00000509419.1:n.*2404C>T
ENST00000689129.1:c.2985C>T	ENSP00000510414.1:p.Ala995=
ENST00000689177.1:n.833C>T
ENST00000689981.1:c.2982C>T	ENSP00000509035.1:p.Ala994=
ENST00000690369.1:n.3000C>T
ENST00000690990.1:c.2976C>T	ENSP00000510461.1:p.Ala992=
ENST00000691233.1:c.2979C>T	ENSP00000509215.1:p.Ala993=
ENST00000691345.1:n.1483C>T
ENST00000691792.1:c.2982C>T	ENSP00000509911.1:p.Ala994=
ENST00000691959.1:n.2861C>T
ENST00000693052.1:c.2982C>T	ENSP00000509558.1:p.Ala994=
ENST00000693440.1:c.2979C>T	ENSP00000509462.1:p.Ala993=
ENST00000693499.1:n.3073C>T
ENST00000380817.8:c.2982C>T MANE Select	ENSP00000370196.2:p.Ala994=
ENST00000348911.10:c.2985C>T	ENSP00000252027.7:p.Ala995=
ENST00000380817.7:c.2982C>T	ENSP00000370196.2:p.Ala994=
NM_002972.3:c.2982C>T	NP_002963.2:p.Ala994=
XM_005261931.1:c.2985C>T	XP_005261988.1:p.Ala995=
XM_005261935.1:c.2982C>T	XP_005261992.1:p.Ala994=
XM_011530707.1:c.3084C>T	XP_011529009.1:p.Ala1028=
XM_011530708.1:c.3036C>T	XP_011529010.1:p.Ala1012=
XM_011530709.1:c.3012C>T	XP_011529011.1:p.Ala1004=
XM_011530710.1:c.3009C>T	XP_011529012.1:p.Ala1003=
XM_011530711.1:c.3087C>T	XP_011529013.1:p.Ala1029=
XR_938344.1:n.3102C>T
NM_001365819.1:c.2985C>T	NP_001352748.1:p.Ala995=
XM_005261935.2:c.2982C>T	XP_005261992.1:p.Ala994=
XM_011530709.2:c.3012C>T	XP_011529011.1:p.Ala1004=
XM_011530710.2:c.3009C>T	XP_011529012.1:p.Ala1003=
XM_017028905.2:c.3012C>T	XP_016884394.1:p.Ala1004=
NM_002972.4:c.2982C>T MANE Select	NP_002963.2:p.Ala994=