Canonical Allele Identifier: CA532430252

Gene: THADA

Linked Data

• dbSNP Id: rs1359290759
• gnomAD v2: 2-43638662-ATATTTTGAACAGCCT-A
• gnomAD v3: 2-43411523-ATATTTTGAACAGCCT-A
• gnomAD v4: 2-43411523-ATATTTTGAACAGCCT-A
• MyVariant Identifiers: chr2:g.43638663_43638677del (hg19) ; chr2:g.43411524_43411538del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43411525_43411539del , CM000664.2:g.43411525_43411539del	GRCh38
NC_000002.11:g.43638664_43638678del , CM000664.1:g.43638664_43638678del	GRCh37
NC_000002.10:g.43492168_43492182del	NCBI36
NG_051580.1:g.189509_189523del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405975.7:c.4059-13399_4059-13385del MANE Select	ENSP00000386088.2:n.4059-13399_4059-13385del
ENST00000398653.5:c.*2975-13399_*2975-13385del	ENSP00000381647.1:n.*2975-13399_*2975-13385del
ENST00000402796.5:c.2465-13399_2465-13385del	ENSP00000385003.1:n.2465-13399_2465-13385del
ENST00000405006.8:c.4059-13399_4059-13385del	ENSP00000385995.4:n.4059-13399_4059-13385del
ENST00000405975.6:c.4059-13399_4059-13385del	ENSP00000386088.2:n.4059-13399_4059-13385del
ENST00000407351.5:c.1778-13399_1778-13385del
ENST00000408045.7:c.*3154-13399_*3154-13385del	ENSP00000384172.2:n.*3154-13399_*3154-13385del
ENST00000485353.5:n.449-13399_449-13385del
NM_001083953.1:c.4059-13399_4059-13385del	NP_001077422.1:n.4059-13399_4059-13385del
NM_022065.4:c.4059-13399_4059-13385del	NP_071348.3:n.4059-13399_4059-13385del
NR_073394.1:n.4009-13399_4009-13385del
XM_006712061.2:c.4059-13399_4059-13385del	XP_006712124.1:n.4059-13399_4059-13385del
XM_006712062.1:c.4056-13399_4056-13385del	XP_006712125.1:n.4056-13399_4056-13385del
XM_006712063.1:c.3939-13399_3939-13385del	XP_006712126.1:n.3939-13399_3939-13385del
XM_006712064.1:c.4059-13399_4059-13385del	XP_006712127.1:n.4059-13399_4059-13385del
XM_006712065.1:c.3837-13399_3837-13385del	XP_006712128.1:n.3837-13399_3837-13385del
XM_006712066.1:c.3696-13399_3696-13385del	XP_006712129.1:n.3696-13399_3696-13385del
XM_006712067.1:c.3693-13399_3693-13385del	XP_006712130.1:n.3693-13399_3693-13385del
XM_006712068.2:c.4059-13399_4059-13385del	XP_006712131.1:n.4059-13399_4059-13385del
XM_006712069.2:c.1608-13399_1608-13385del	XP_006712132.1:n.1608-13399_1608-13385del
XM_011533016.1:c.1371-13399_1371-13385del	XP_011531318.1:n.1371-13399_1371-13385del
NM_001345923.1:c.4056-13399_4056-13385del	NP_001332852.1:n.4056-13399_4056-13385del
NM_001345924.1:c.3936-13399_3936-13385del	NP_001332853.1:n.3936-13399_3936-13385del
NM_001345925.1:c.4059-13399_4059-13385del	NP_001332854.1:n.4059-13399_4059-13385del
NR_144316.1:n.4199-13399_4199-13385del
XM_006712064.2:c.4059-13399_4059-13385del	XP_006712127.1:n.4059-13399_4059-13385del
XM_006712068.3:c.4059-13399_4059-13385del	XP_006712131.1:n.4059-13399_4059-13385del
XM_006712069.3:c.1608-13399_1608-13385del	XP_006712132.1:n.1608-13399_1608-13385del
XM_017004675.1:c.1371-13399_1371-13385del	XP_016860164.1:n.1371-13399_1371-13385del
NM_001083953.2:c.4059-13399_4059-13385del	NP_001077422.1:n.4059-13399_4059-13385del
NM_001345923.2:c.4056-13399_4056-13385del	NP_001332852.1:n.4056-13399_4056-13385del
NM_001345924.2:c.3936-13399_3936-13385del	NP_001332853.1:n.3936-13399_3936-13385del
NM_001345925.2:c.4059-13399_4059-13385del	NP_001332854.1:n.4059-13399_4059-13385del
NM_022065.5:c.4059-13399_4059-13385del MANE Select	NP_071348.3:n.4059-13399_4059-13385del
NR_073394.2:n.4001-13399_4001-13385del
NR_144316.2:n.4191-13399_4191-13385del