Canonical Allele Identifier: CA13775896

Gene: TRHDE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.72331215G>T , CM000674.2:g.72331215G>T	GRCh38
NC_000012.11:g.72724995G>T , CM000674.1:g.72724995G>T	GRCh37
NC_000012.10:g.71011262G>T	NCBI36
NG_046971.1:g.63636G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261180.10:c.1188+44261G>T MANE Select	ENSP00000261180.5:n.1188+44261G>T
ENST00000547300.2:c.1188+44261G>T	ENSP00000447822.2:n.1188+44261G>T
ENST00000261180.9:c.1053+44261G>T	ENSP00000261180.4:n.1053+44261G>T
ENST00000261180.8:c.1053+44261G>T	ENSP00000261180.4:n.1053+44261G>T
ENST00000547300.1:c.349+44261G>T
ENST00000548156.1:n.280-46780G>T
NM_013381.2:c.1053+44261G>T	NP_037513.1:n.1053+44261G>T
XM_005268819.3:c.1188+44261G>T	XP_005268876.1:n.1188+44261G>T
XR_944529.1:n.1251+44261G>T
XM_005268819.5:c.1053+44261G>T	XP_005268876.2:n.1053+44261G>T
XM_017019243.2:c.1053+44261G>T	XP_016874732.2:n.1053+44261G>T
XM_017019244.1:c.144+44261G>T	XP_016874733.1:n.144+44261G>T
NM_013381.3:c.1188+44261G>T MANE Select	NP_037513.2:n.1188+44261G>T