Canonical Allele Identifier: CA1167907641

Gene: DHCR24

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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