Canonical Allele Identifier: CA769047847

Gene: THADA

Linked Data

• dbSNP Id: rs1297509232
• MyVariant Identifiers: chr2:g.43638740A>G (hg19) ; chr2:g.43411601A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43411601A>G , CM000664.2:g.43411601A>G	GRCh38
NC_000002.11:g.43638740A>G , CM000664.1:g.43638740A>G	GRCh37
NC_000002.10:g.43492244A>G	NCBI36
NG_051580.1:g.189446T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405975.7:c.4059-13462T>C MANE Select	ENSP00000386088.2:n.4059-13462T>C
ENST00000398653.5:c.*2975-13462T>C	ENSP00000381647.1:n.*2975-13462T>C
ENST00000402796.5:c.2465-13462T>C	ENSP00000385003.1:n.2465-13462T>C
ENST00000405006.8:c.4059-13462T>C	ENSP00000385995.4:n.4059-13462T>C
ENST00000405975.6:c.4059-13462T>C	ENSP00000386088.2:n.4059-13462T>C
ENST00000407351.5:c.1778-13462T>C
ENST00000408045.7:c.*3154-13462T>C	ENSP00000384172.2:n.*3154-13462T>C
ENST00000485353.5:n.449-13462T>C
NM_001083953.1:c.4059-13462T>C	NP_001077422.1:n.4059-13462T>C
NM_022065.4:c.4059-13462T>C	NP_071348.3:n.4059-13462T>C
NR_073394.1:n.4009-13462T>C
XM_006712061.2:c.4059-13462T>C	XP_006712124.1:n.4059-13462T>C
XM_006712062.1:c.4056-13462T>C	XP_006712125.1:n.4056-13462T>C
XM_006712063.1:c.3939-13462T>C	XP_006712126.1:n.3939-13462T>C
XM_006712064.1:c.4059-13462T>C	XP_006712127.1:n.4059-13462T>C
XM_006712065.1:c.3837-13462T>C	XP_006712128.1:n.3837-13462T>C
XM_006712066.1:c.3696-13462T>C	XP_006712129.1:n.3696-13462T>C
XM_006712067.1:c.3693-13462T>C	XP_006712130.1:n.3693-13462T>C
XM_006712068.2:c.4059-13462T>C	XP_006712131.1:n.4059-13462T>C
XM_006712069.2:c.1608-13462T>C	XP_006712132.1:n.1608-13462T>C
XM_011533016.1:c.1371-13462T>C	XP_011531318.1:n.1371-13462T>C
NM_001345923.1:c.4056-13462T>C	NP_001332852.1:n.4056-13462T>C
NM_001345924.1:c.3936-13462T>C	NP_001332853.1:n.3936-13462T>C
NM_001345925.1:c.4059-13462T>C	NP_001332854.1:n.4059-13462T>C
NR_144316.1:n.4199-13462T>C
XM_006712064.2:c.4059-13462T>C	XP_006712127.1:n.4059-13462T>C
XM_006712068.3:c.4059-13462T>C	XP_006712131.1:n.4059-13462T>C
XM_006712069.3:c.1608-13462T>C	XP_006712132.1:n.1608-13462T>C
XM_017004675.1:c.1371-13462T>C	XP_016860164.1:n.1371-13462T>C
NM_001083953.2:c.4059-13462T>C	NP_001077422.1:n.4059-13462T>C
NM_001345923.2:c.4056-13462T>C	NP_001332852.1:n.4056-13462T>C
NM_001345924.2:c.3936-13462T>C	NP_001332853.1:n.3936-13462T>C
NM_001345925.2:c.4059-13462T>C	NP_001332854.1:n.4059-13462T>C
NM_022065.5:c.4059-13462T>C MANE Select	NP_071348.3:n.4059-13462T>C
NR_073394.2:n.4001-13462T>C
NR_144316.2:n.4191-13462T>C