Canonical Allele Identifier: CA2581766420

Gene: THADA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43579779C>G , CM000664.2:g.43579779C>G	GRCh38
NC_000002.11:g.43806918C>G , CM000664.1:g.43806918C>G	GRCh37
NC_000002.10:g.43660422C>G	NCBI36
NG_051580.1:g.21268G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405975.7:c.722-1172G>C MANE Select	ENSP00000386088.2:n.722-1172G>C
ENST00000398653.5:c.722-1172G>C	ENSP00000381647.1:n.722-1172G>C
ENST00000402360.6:c.722-1172G>C	ENSP00000385441.2:n.722-1172G>C
ENST00000403856.1:c.722-1172G>C	ENSP00000385469.1:n.722-1172G>C
ENST00000404790.5:c.722-1172G>C	ENSP00000384266.1:n.722-1172G>C
ENST00000405006.8:c.722-1172G>C	ENSP00000385995.4:n.722-1172G>C
ENST00000405975.6:c.722-1172G>C	ENSP00000386088.2:n.722-1172G>C
ENST00000408045.7:c.722-1172G>C	ENSP00000384172.2:n.722-1172G>C
ENST00000474159.6:c.722-1172G>C	ENSP00000445294.1:n.722-1172G>C
NM_001083953.1:c.722-1172G>C	NP_001077422.1:n.722-1172G>C
NM_001271643.1:c.722-1172G>C	NP_001258572.1:n.722-1172G>C
NM_001271644.1:c.722-1172G>C	NP_001258573.1:n.722-1172G>C
NM_022065.4:c.722-1172G>C	NP_071348.3:n.722-1172G>C
NR_073394.1:n.862-1172G>C
XM_006712061.2:c.722-1172G>C	XP_006712124.1:n.722-1172G>C
XM_006712062.1:c.722-1172G>C	XP_006712125.1:n.722-1172G>C
XM_006712063.1:c.722-1172G>C	XP_006712126.1:n.722-1172G>C
XM_006712064.1:c.722-1172G>C	XP_006712127.1:n.722-1172G>C
XM_006712065.1:c.722-1172G>C	XP_006712128.1:n.722-1172G>C
XM_006712066.1:c.722-1172G>C	XP_006712129.1:n.722-1172G>C
XM_006712067.1:c.722-1172G>C	XP_006712130.1:n.722-1172G>C
XM_006712068.2:c.722-1172G>C	XP_006712131.1:n.722-1172G>C
XM_011533015.1:c.722-1172G>C	XP_011531317.1:n.722-1172G>C
NM_001345923.1:c.722-1172G>C	NP_001332852.1:n.722-1172G>C
NM_001345924.1:c.722-1172G>C	NP_001332853.1:n.722-1172G>C
NM_001345925.1:c.722-1172G>C	NP_001332854.1:n.722-1172G>C
NR_144316.1:n.862-1172G>C
XM_006712064.2:c.722-1172G>C	XP_006712127.1:n.722-1172G>C
XM_006712068.3:c.722-1172G>C	XP_006712131.1:n.722-1172G>C
XM_011533015.3:c.722-1172G>C	XP_011531317.1:n.722-1172G>C
XM_017004675.1:c.-1756-1172G>C	XP_016860164.1:n.-1756-1172G>C
NM_001271643.2:c.722-1172G>C	NP_001258572.1:n.722-1172G>C
NM_001271644.2:c.722-1172G>C	NP_001258573.1:n.722-1172G>C
NM_001083953.2:c.722-1172G>C	NP_001077422.1:n.722-1172G>C
NM_001345923.2:c.722-1172G>C	NP_001332852.1:n.722-1172G>C
NM_001345924.2:c.722-1172G>C	NP_001332853.1:n.722-1172G>C
NM_001345925.2:c.722-1172G>C	NP_001332854.1:n.722-1172G>C
NM_022065.5:c.722-1172G>C MANE Select	NP_071348.3:n.722-1172G>C
NR_073394.2:n.854-1172G>C
NR_144316.2:n.854-1172G>C