Canonical Allele Identifier: CA1141698667

Gene: HES4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.999691C= , CM000663.2:g.999691C=	GRCh38
NC_000001.10:g.935071C= , CM000663.1:g.935071C=	GRCh37
NC_000001.9:g.924934C=	NCBI36
NG_033033.2:g.3554C=

Transcript Alleles

HGVS	Amino-acid Change
NM_021170.4:c.204+1G= MANE Select	NP_066993.1:n.204+1G=
ENST00000304952.11:c.204+1G= MANE Select	ENSP00000304595.7:n.204+1G=
NM_001142467.1:c.282+1G=	NP_001135939.1:n.282+1G=
NM_001142467.2:c.282+1G=	NP_001135939.1:n.282+1G=
NM_021170.3:c.204+1G=	NP_066993.1:n.204+1G=
ENST00000304952.10:c.204+1G=	ENSP00000304595.6:n.204+1G=
ENST00000428771.6:c.282+1G=	ENSP00000393198.2:n.282+1G=
ENST00000481869.1:n.406G=
ENST00000484667.2:c.109-78G=	ENSP00000425085.1:n.109-78G=
XM_005244771.3:c.109-78G=	XP_005244828.1:n.109-78G=
XM_005244771.4:c.109-78G=	XP_005244828.1:n.109-78G=
XM_011541868.1:c.282+1G=	XP_011540170.1:n.282+1G=