Canonical Allele Identifier: CA2493672753

Gene: THADA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43326810T= , CM000664.2:g.43326810T=	GRCh38
NC_000002.11:g.43553949T= , CM000664.1:g.43553949T=	GRCh37
NC_000002.10:g.43407453T=	NCBI36
NG_051580.1:g.274237A=

Transcript Alleles

HGVS	Amino-acid Change
NM_022065.5:c.4344-6270A= MANE Select	NP_071348.3:n.4344-6270A=
ENST00000405975.7:c.4344-6270A= MANE Select	ENSP00000386088.2:n.4344-6270A=
NM_001083953.1:c.4344-6270A=	NP_001077422.1:n.4344-6270A=
NM_001083953.2:c.4344-6270A=	NP_001077422.1:n.4344-6270A=
NM_001345923.1:c.4341-6270A=	NP_001332852.1:n.4341-6270A=
NM_001345923.2:c.4341-6270A=	NP_001332852.1:n.4341-6270A=
NM_001345924.1:c.4221-6270A=	NP_001332853.1:n.4221-6270A=
NM_001345924.2:c.4221-6270A=	NP_001332853.1:n.4221-6270A=
NM_001345925.1:c.4344-6270A=	NP_001332854.1:n.4344-6270A=
NM_001345925.2:c.4344-6270A=	NP_001332854.1:n.4344-6270A=
NM_022065.4:c.4344-6270A=	NP_071348.3:n.4344-6270A=
NR_073394.1:n.4294-6270A=
NR_073394.2:n.4286-6270A=
NR_144316.1:n.4368-6270A=
NR_144316.2:n.4360-6270A=
ENST00000398653.5:c.*3260-6270A=	ENSP00000381647.1:n.*3260-6270A=
ENST00000405006.8:c.4344-6270A=	ENSP00000385995.4:n.4344-6270A=
ENST00000405975.6:c.4344-6270A=	ENSP00000386088.2:n.4344-6270A=
ENST00000407351.5:c.2063-6270A=
ENST00000486735.5:n.248-6270A=
XM_006712061.2:c.4344-6270A=	XP_006712124.1:n.4344-6270A=
XM_006712062.1:c.4341-6270A=	XP_006712125.1:n.4341-6270A=
XM_006712063.1:c.4224-6270A=	XP_006712126.1:n.4224-6270A=
XM_006712064.1:c.4344-6270A=	XP_006712127.1:n.4344-6270A=
XM_006712064.2:c.4344-6270A=	XP_006712127.1:n.4344-6270A=
XM_006712065.1:c.4122-6270A=	XP_006712128.1:n.4122-6270A=
XM_006712066.1:c.3981-6270A=	XP_006712129.1:n.3981-6270A=
XM_006712067.1:c.3978-6270A=	XP_006712130.1:n.3978-6270A=
XM_006712069.2:c.1893-6270A=	XP_006712132.1:n.1893-6270A=
XM_006712069.3:c.1893-6270A=	XP_006712132.1:n.1893-6270A=
XM_011533016.1:c.1656-6270A=	XP_011531318.1:n.1656-6270A=
XM_017004675.1:c.1656-6270A=	XP_016860164.1:n.1656-6270A=