Canonical Allele Identifier: CA1180976040

Gene: DIPK1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92936235G= , CM000663.2:g.92936235G=	GRCh38
NC_000001.10:g.93401792G= , CM000663.1:g.93401792G=	GRCh37
NC_000001.9:g.93174380G=	NCBI36
NG_033051.1:g.30288C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370310.5:c.54+25141C= MANE Select	ENSP00000359333.4:n.54+25141C=
ENST00000370310.4:c.54+25141C=	ENSP00000359333.4:n.54+25141C=
ENST00000613902.4:c.54+25141C=	ENSP00000484866.1:n.54+25141C=
ENST00000615519.4:c.54+25141C=	ENSP00000483279.1:n.54+25141C=
ENST00000616709.4:c.54+25141C=	ENSP00000482718.1:n.54+25141C=
NM_001006605.4:c.54+25141C=	NP_001006606.2:n.54+25141C=
NM_001252269.1:c.54+25141C=	NP_001239198.1:n.54+25141C=
NM_001252270.1:c.54+25141C=	NP_001239199.1:n.54+25141C=
NM_001252273.1:c.54+25141C=	NP_001239202.1:n.54+25141C=
NM_001006605.5:c.54+25141C= MANE Select	NP_001006606.2:n.54+25141C=
NM_001252269.2:c.54+25141C=	NP_001239198.1:n.54+25141C=
NM_001252270.2:c.54+25141C=	NP_001239199.1:n.54+25141C=
NM_001252273.2:c.54+25141C=	NP_001239202.1:n.54+25141C=