Canonical Allele Identifier: CA2034981910

Gene: DHH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49089919C= , CM000674.2:g.49089919C=	GRCh38
NC_000012.11:g.49483702C= , CM000674.1:g.49483702C=	GRCh37
NC_000012.10:g.47769969C=	NCBI36
NG_008973.1:g.9901G=
NG_008973.2:g.9901G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000649637.2:c.1131G= MANE Select	ENSP00000497483.1:p.Pro377=
ENST00000266991.2:c.1131G=	ENSP00000266991.2:p.Pro377=
NM_021044.2:c.1131G=	NP_066382.1:p.Pro377=
NM_021044.4:c.1131G= MANE Select	NP_066382.1:p.Pro377=
XM_017019380.1:c.990G=	XP_016874869.1:p.Pro330=
XM_017019381.1:c.789G=	XP_016874870.1:p.Pro263=