Canonical Allele Identifier: CA2493715085

Gene: THADA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43411738_43411741delinsAAAT , CM000664.2:g.43411738_43411741delinsAAAT	GRCh38
NC_000002.11:g.43638877_43638880delinsAAAT , CM000664.1:g.43638877_43638880delinsAAAT	GRCh37
NC_000002.10:g.43492381_43492384delinsAAAT	NCBI36
NG_051580.1:g.189306_189309delinsATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405975.7:c.4059-13602_4059-13599delinsATTT MANE Select	ENSP00000386088.2:n.4059-13602_4059-13599delinsATTT
ENST00000398653.5:c.*2975-13602_*2975-13599delinsATTT	ENSP00000381647.1:n.*2975-13602_*2975-13599delinsATTT
ENST00000402796.5:c.2465-13602_2465-13599delinsATTT	ENSP00000385003.1:n.2465-13602_2465-13599delinsATTT
ENST00000405006.8:c.4059-13602_4059-13599delinsATTT	ENSP00000385995.4:n.4059-13602_4059-13599delinsATTT
ENST00000405975.6:c.4059-13602_4059-13599delinsATTT	ENSP00000386088.2:n.4059-13602_4059-13599delinsATTT
ENST00000407351.5:c.1778-13602_1778-13599delinsATTT
ENST00000408045.7:c.*3154-13602_*3154-13599delinsATTT	ENSP00000384172.2:n.*3154-13602_*3154-13599delinsATTT
ENST00000485353.5:n.449-13602_449-13599delinsATTT
NM_001083953.1:c.4059-13602_4059-13599delinsATTT	NP_001077422.1:n.4059-13602_4059-13599delinsATTT
NM_022065.4:c.4059-13602_4059-13599delinsATTT	NP_071348.3:n.4059-13602_4059-13599delinsATTT
NR_073394.1:n.4009-13602_4009-13599delinsATTT
XM_006712061.2:c.4059-13602_4059-13599delinsATTT	XP_006712124.1:n.4059-13602_4059-13599delinsATTT
XM_006712062.1:c.4056-13602_4056-13599delinsATTT	XP_006712125.1:n.4056-13602_4056-13599delinsATTT
XM_006712063.1:c.3939-13602_3939-13599delinsATTT	XP_006712126.1:n.3939-13602_3939-13599delinsATTT
XM_006712064.1:c.4059-13602_4059-13599delinsATTT	XP_006712127.1:n.4059-13602_4059-13599delinsATTT
XM_006712065.1:c.3837-13602_3837-13599delinsATTT	XP_006712128.1:n.3837-13602_3837-13599delinsATTT
XM_006712066.1:c.3696-13602_3696-13599delinsATTT	XP_006712129.1:n.3696-13602_3696-13599delinsATTT
XM_006712067.1:c.3693-13602_3693-13599delinsATTT	XP_006712130.1:n.3693-13602_3693-13599delinsATTT
XM_006712068.2:c.4059-13602_4059-13599delinsATTT	XP_006712131.1:n.4059-13602_4059-13599delinsATTT
XM_006712069.2:c.1608-13602_1608-13599delinsATTT	XP_006712132.1:n.1608-13602_1608-13599delinsATTT
XM_011533016.1:c.1371-13602_1371-13599delinsATTT	XP_011531318.1:n.1371-13602_1371-13599delinsATTT
NM_001345923.1:c.4056-13602_4056-13599delinsATTT	NP_001332852.1:n.4056-13602_4056-13599delinsATTT
NM_001345924.1:c.3936-13602_3936-13599delinsATTT	NP_001332853.1:n.3936-13602_3936-13599delinsATTT
NM_001345925.1:c.4059-13602_4059-13599delinsATTT	NP_001332854.1:n.4059-13602_4059-13599delinsATTT
NR_144316.1:n.4199-13602_4199-13599delinsATTT
XM_006712064.2:c.4059-13602_4059-13599delinsATTT	XP_006712127.1:n.4059-13602_4059-13599delinsATTT
XM_006712068.3:c.4059-13602_4059-13599delinsATTT	XP_006712131.1:n.4059-13602_4059-13599delinsATTT
XM_006712069.3:c.1608-13602_1608-13599delinsATTT	XP_006712132.1:n.1608-13602_1608-13599delinsATTT
XM_017004675.1:c.1371-13602_1371-13599delinsATTT	XP_016860164.1:n.1371-13602_1371-13599delinsATTT
NM_001083953.2:c.4059-13602_4059-13599delinsATTT	NP_001077422.1:n.4059-13602_4059-13599delinsATTT
NM_001345923.2:c.4056-13602_4056-13599delinsATTT	NP_001332852.1:n.4056-13602_4056-13599delinsATTT
NM_001345924.2:c.3936-13602_3936-13599delinsATTT	NP_001332853.1:n.3936-13602_3936-13599delinsATTT
NM_001345925.2:c.4059-13602_4059-13599delinsATTT	NP_001332854.1:n.4059-13602_4059-13599delinsATTT
NM_022065.5:c.4059-13602_4059-13599delinsATTT MANE Select	NP_071348.3:n.4059-13602_4059-13599delinsATTT
NR_073394.2:n.4001-13602_4001-13599delinsATTT
NR_144316.2:n.4191-13602_4191-13599delinsATTT