Canonical Allele Identifier: CA1140495629

Gene: DHCR24

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54852372T= , CM000663.2:g.54852372T=	GRCh38
NC_000001.10:g.55318045T= , CM000663.1:g.55318045T=	GRCh37
NC_000001.9:g.55090633T=	NCBI36
NG_008839.1:g.39877A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371269.9:c.1412A= MANE Select	ENSP00000360316.3:p.Tyr471=
ENST00000436604.2:c.1412A=	ENSP00000416585.2:p.Tyr471=
ENST00000535035.6:c.1448A=	ENSP00000440191.3:p.Tyr483=
ENST00000647585.1:n.1216A=
ENST00000647912.1:c.*1047A=	ENSP00000497559.1:n.*1047A=
ENST00000648712.1:n.1530A=
ENST00000648728.1:c.*1067A=	ENSP00000497084.1:n.*1067A=
ENST00000649769.1:c.*2114A=	ENSP00000498012.1:n.*2114A=
ENST00000371269.7:c.1412A=	ENSP00000360316.3:p.Tyr471=
ENST00000436604.1:c.324A=
ENST00000535035.5:c.1145A=	ENSP00000440191.2:p.Tyr382=
NM_014762.3:c.1412A=	NP_055577.1:p.Tyr471=
NM_014762.4:c.1412A= MANE Select	NP_055577.1:p.Tyr471=