Canonical Allele Identifier: CA2045712231

Gene: TRHDE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.72330171A= , CM000674.2:g.72330171A=	GRCh38
NC_000012.11:g.72723951A= , CM000674.1:g.72723951A=	GRCh37
NC_000012.10:g.71010218A=	NCBI36
NG_046971.1:g.62592A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261180.10:c.1188+43217A= MANE Select	ENSP00000261180.5:n.1188+43217A=
ENST00000547300.2:c.1188+43217A=	ENSP00000447822.2:n.1188+43217A=
ENST00000261180.9:c.1053+43217A=	ENSP00000261180.4:n.1053+43217A=
ENST00000261180.8:c.1053+43217A=	ENSP00000261180.4:n.1053+43217A=
ENST00000547300.1:c.349+43217A=
ENST00000548156.1:n.280-47824A=
NM_013381.2:c.1053+43217A=	NP_037513.1:n.1053+43217A=
XM_005268819.3:c.1188+43217A=	XP_005268876.1:n.1188+43217A=
XR_944529.1:n.1251+43217A=
XM_005268819.5:c.1053+43217A=	XP_005268876.2:n.1053+43217A=
XM_017019243.2:c.1053+43217A=	XP_016874732.2:n.1053+43217A=
XM_017019244.1:c.144+43217A=	XP_016874733.1:n.144+43217A=
NM_013381.3:c.1188+43217A= MANE Select	NP_037513.2:n.1188+43217A=