Canonical Allele Identifier: CA2493763299

Gene: THADA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43505684T= , CM000664.2:g.43505684T=	GRCh38
NC_000002.11:g.43732823T= , CM000664.1:g.43732823T=	GRCh37
NC_000002.10:g.43586327T=	NCBI36
NG_051580.1:g.95363A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405975.7:c.3559A= MANE Select	ENSP00000386088.2:p.Thr1187=
ENST00000398653.5:c.*2657A=	ENSP00000381647.1:n.*2657A=
ENST00000402796.5:c.2097A=	ENSP00000385003.1:n.2097A=
ENST00000405006.8:c.3559A=	ENSP00000385995.4:p.Thr1187=
ENST00000405975.6:c.3559A=	ENSP00000386088.2:p.Thr1187=
ENST00000407351.5:c.1500A=
ENST00000408045.7:c.*2654A=	ENSP00000384172.2:n.*2654A=
ENST00000436947.1:n.158A=
NM_001083953.1:c.3559A=	NP_001077422.1:p.Thr1187=
NM_022065.4:c.3559A=	NP_071348.3:p.Thr1187=
NR_073394.1:n.3691A=
XM_006712061.2:c.3559A=	XP_006712124.1:p.Thr1187=
XM_006712062.1:c.3556A=	XP_006712125.1:p.Thr1186=
XM_006712063.1:c.3439A=	XP_006712126.1:p.Thr1147=
XM_006712064.1:c.3559A=	XP_006712127.1:p.Thr1187=
XM_006712065.1:c.3559A=	XP_006712128.1:p.Thr1187=
XM_006712066.1:c.3196A=	XP_006712129.1:p.Thr1066=
XM_006712067.1:c.3193A=	XP_006712130.1:p.Thr1065=
XM_006712068.2:c.3559A=	XP_006712131.1:p.Thr1187=
XM_006712069.2:c.1108A=	XP_006712132.1:p.Thr370=
XM_011533015.1:c.3559A=	XP_011531317.1:p.Thr1187=
XM_011533016.1:c.871A=	XP_011531318.1:p.Thr291=
NM_001345923.1:c.3556A=	NP_001332852.1:p.Thr1186=
NM_001345924.1:c.3436A=	NP_001332853.1:p.Thr1146=
NM_001345925.1:c.3559A=	NP_001332854.1:p.Thr1187=
NR_144316.1:n.3699A=
XM_006712064.2:c.3559A=	XP_006712127.1:p.Thr1187=
XM_006712068.3:c.3559A=	XP_006712131.1:p.Thr1187=
XM_006712069.3:c.1108A=	XP_006712132.1:p.Thr370=
XM_011533015.3:c.3559A=	XP_011531317.1:p.Thr1187=
XM_017004675.1:c.871A=	XP_016860164.1:p.Thr291=
NM_001083953.2:c.3559A=	NP_001077422.1:p.Thr1187=
NM_001345923.2:c.3556A=	NP_001332852.1:p.Thr1186=
NM_001345924.2:c.3436A=	NP_001332853.1:p.Thr1146=
NM_001345925.2:c.3559A=	NP_001332854.1:p.Thr1187=
NM_022065.5:c.3559A= MANE Select	NP_071348.3:p.Thr1187=
NR_073394.2:n.3683A=
NR_144316.2:n.3691A=