Canonical Allele Identifier: CA1139827047

Gene: DHCR24

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54854229A= , CM000663.2:g.54854229A=	GRCh38
NC_000001.10:g.55319902A= , CM000663.1:g.55319902A=	GRCh37
NC_000001.9:g.55092490A=	NCBI36
NG_008839.1:g.38020T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371269.9:c.1026T= MANE Select	ENSP00000360316.3:p.Ile342=
ENST00000436604.2:c.1026T=	ENSP00000416585.2:p.Ile342=
ENST00000535035.6:c.1062T=	ENSP00000440191.3:p.Ile354=
ENST00000647585.1:n.830T=
ENST00000647912.1:c.*661T=	ENSP00000497559.1:n.*661T=
ENST00000648712.1:n.1144T=
ENST00000648728.1:c.*681T=	ENSP00000497084.1:n.*681T=
ENST00000649769.1:c.*681T=	ENSP00000498012.1:n.*681T=
ENST00000371269.7:c.1026T=	ENSP00000360316.3:p.Ile342=
ENST00000535035.5:c.759T=	ENSP00000440191.2:p.Ile253=
NM_014762.3:c.1026T=	NP_055577.1:p.Ile342=
NM_014762.4:c.1026T= MANE Select	NP_055577.1:p.Ile342=