Canonical Allele Identifier: CA2034981912

Gene: DHH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49089925G= , CM000674.2:g.49089925G=	GRCh38
NC_000012.11:g.49483708G= , CM000674.1:g.49483708G=	GRCh37
NC_000012.10:g.47769975G=	NCBI36
NG_008973.1:g.9895C=
NG_008973.2:g.9895C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000649637.2:c.1125C= MANE Select	ENSP00000497483.1:p.Val375=
ENST00000266991.2:c.1125C=	ENSP00000266991.2:p.Val375=
NM_021044.2:c.1125C=	NP_066382.1:p.Val375=
NM_021044.4:c.1125C= MANE Select	NP_066382.1:p.Val375=
XM_017019380.1:c.984C=	XP_016874869.1:p.Val328=
XM_017019381.1:c.783C=	XP_016874870.1:p.Val261=