Canonical Allele Identifier: CA1139818136

Gene: DHCR24

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54876242T= , CM000663.2:g.54876242T=	GRCh38
NC_000001.10:g.55341915T= , CM000663.1:g.55341915T=	GRCh37
NC_000001.9:g.55114503T=	NCBI36
NG_008839.1:g.16007A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371269.9:c.388-195A= MANE Select	ENSP00000360316.3:n.388-195A=
ENST00000436604.2:c.388-195A=	ENSP00000416585.2:n.388-195A=
ENST00000535035.6:c.388-195A=	ENSP00000440191.3:n.388-195A=
ENST00000647585.1:n.192-195A=
ENST00000647912.1:c.*23-195A=	ENSP00000497559.1:n.*23-195A=
ENST00000648182.1:c.265-195A=	ENSP00000498045.1:n.265-195A=
ENST00000648494.1:n.511-195A=
ENST00000648641.1:n.234-195A=
ENST00000648712.1:n.506-195A=
ENST00000648728.1:c.*43-195A=	ENSP00000497084.1:n.*43-195A=
ENST00000649769.1:c.*43-195A=	ENSP00000498012.1:n.*43-195A=
ENST00000650362.1:c.121-195A=	ENSP00000497612.1:n.121-195A=
ENST00000371269.7:c.388-195A=	ENSP00000360316.3:n.388-195A=
ENST00000535035.5:c.121-195A=	ENSP00000440191.2:n.121-195A=
NM_014762.3:c.388-195A=	NP_055577.1:n.388-195A=
NM_014762.4:c.388-195A= MANE Select	NP_055577.1:n.388-195A=