Canonical Allele Identifier: CA691655042

Gene: TRHDE

Linked Data

• dbSNP Id: rs12831974
• MyVariant Identifiers: chr12:g.72724034T>A (hg19) ; chr12:g.72330254T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.72330254T>A , CM000674.2:g.72330254T>A	GRCh38
NC_000012.11:g.72724034T>A , CM000674.1:g.72724034T>A	GRCh37
NC_000012.10:g.71010301T>A	NCBI36
NG_046971.1:g.62675T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261180.10:c.1188+43300T>A MANE Select	ENSP00000261180.5:n.1188+43300T>A
ENST00000547300.2:c.1188+43300T>A	ENSP00000447822.2:n.1188+43300T>A
ENST00000261180.9:c.1053+43300T>A	ENSP00000261180.4:n.1053+43300T>A
ENST00000261180.8:c.1053+43300T>A	ENSP00000261180.4:n.1053+43300T>A
ENST00000547300.1:c.349+43300T>A
ENST00000548156.1:n.280-47741T>A
NM_013381.2:c.1053+43300T>A	NP_037513.1:n.1053+43300T>A
XM_005268819.3:c.1188+43300T>A	XP_005268876.1:n.1188+43300T>A
XR_944529.1:n.1251+43300T>A
XM_005268819.5:c.1053+43300T>A	XP_005268876.2:n.1053+43300T>A
XM_017019243.2:c.1053+43300T>A	XP_016874732.2:n.1053+43300T>A
XM_017019244.1:c.144+43300T>A	XP_016874733.1:n.144+43300T>A
NM_013381.3:c.1188+43300T>A MANE Select	NP_037513.2:n.1188+43300T>A