Canonical Allele Identifier: CA532431736

Gene: THADA

Linked Data

• dbSNP Id: rs747436206
• gnomAD v2: 2-43732727-C-A
• gnomAD v4: 2-43505588-C-A
• MyVariant Identifiers: chr2:g.43732727C>A (hg19) ; chr2:g.43505588C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43505588C>A , CM000664.2:g.43505588C>A	GRCh38
NC_000002.11:g.43732727C>A , CM000664.1:g.43732727C>A	GRCh37
NC_000002.10:g.43586231C>A	NCBI36
NG_051580.1:g.95459G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405975.7:c.3621+34G>T MANE Select	ENSP00000386088.2:n.3621+34G>T
ENST00000398653.5:c.*2719+34G>T	ENSP00000381647.1:n.*2719+34G>T
ENST00000402796.5:c.2159+34G>T	ENSP00000385003.1:n.2159+34G>T
ENST00000405006.8:c.3621+34G>T	ENSP00000385995.4:n.3621+34G>T
ENST00000405975.6:c.3621+34G>T	ENSP00000386088.2:n.3621+34G>T
ENST00000407351.5:c.1562+34G>T
ENST00000408045.7:c.*2716+34G>T	ENSP00000384172.2:n.*2716+34G>T
ENST00000436947.1:n.220+34G>T
NM_001083953.1:c.3621+34G>T	NP_001077422.1:n.3621+34G>T
NM_022065.4:c.3621+34G>T	NP_071348.3:n.3621+34G>T
NR_073394.1:n.3753+34G>T
XM_006712061.2:c.3621+34G>T	XP_006712124.1:n.3621+34G>T
XM_006712062.1:c.3618+34G>T	XP_006712125.1:n.3618+34G>T
XM_006712063.1:c.3501+34G>T	XP_006712126.1:n.3501+34G>T
XM_006712064.1:c.3621+34G>T	XP_006712127.1:n.3621+34G>T
XM_006712065.1:c.3621+34G>T	XP_006712128.1:n.3621+34G>T
XM_006712066.1:c.3258+34G>T	XP_006712129.1:n.3258+34G>T
XM_006712067.1:c.3255+34G>T	XP_006712130.1:n.3255+34G>T
XM_006712068.2:c.3621+34G>T	XP_006712131.1:n.3621+34G>T
XM_006712069.2:c.1170+34G>T	XP_006712132.1:n.1170+34G>T
XM_011533015.1:c.3621+34G>T	XP_011531317.1:n.3621+34G>T
XM_011533016.1:c.933+34G>T	XP_011531318.1:n.933+34G>T
NM_001345923.1:c.3618+34G>T	NP_001332852.1:n.3618+34G>T
NM_001345924.1:c.3498+34G>T	NP_001332853.1:n.3498+34G>T
NM_001345925.1:c.3621+34G>T	NP_001332854.1:n.3621+34G>T
NR_144316.1:n.3761+34G>T
XM_006712064.2:c.3621+34G>T	XP_006712127.1:n.3621+34G>T
XM_006712068.3:c.3621+34G>T	XP_006712131.1:n.3621+34G>T
XM_006712069.3:c.1170+34G>T	XP_006712132.1:n.1170+34G>T
XM_011533015.3:c.3621+34G>T	XP_011531317.1:n.3621+34G>T
XM_017004675.1:c.933+34G>T	XP_016860164.1:n.933+34G>T
NM_001083953.2:c.3621+34G>T	NP_001077422.1:n.3621+34G>T
NM_001345923.2:c.3618+34G>T	NP_001332852.1:n.3618+34G>T
NM_001345924.2:c.3498+34G>T	NP_001332853.1:n.3498+34G>T
NM_001345925.2:c.3621+34G>T	NP_001332854.1:n.3621+34G>T
NM_022065.5:c.3621+34G>T MANE Select	NP_071348.3:n.3621+34G>T
NR_073394.2:n.3745+34G>T
NR_144316.2:n.3753+34G>T