Canonical Allele Identifier: CA22759850
Gene: DHCR24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54867852C>A , CM000663.2:g.54867852C>A GRCh38
NC_000001.10:g.55333525C>A , CM000663.1:g.55333525C>A GRCh37
NC_000001.9:g.55106113C>A NCBI36
NG_008839.1:g.24397G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371269.9:c.877-2406G>T MANE Select ENSP00000360316.3:n.877-2406G>T
ENST00000436604.2:c.877-2406G>T ENSP00000416585.2:n.877-2406G>T
ENST00000535035.6:c.877-2406G>T ENSP00000440191.3:n.877-2406G>T
ENST00000647585.1:n.681-2406G>T
ENST00000647912.1:c.*512-2406G>T ENSP00000497559.1:n.*512-2406G>T
ENST00000648712.1:n.995-2406G>T
ENST00000648728.1:c.*532-2406G>T ENSP00000497084.1:n.*532-2406G>T
ENST00000649769.1:c.*532-2406G>T ENSP00000498012.1:n.*532-2406G>T
ENST00000371269.7:c.877-2406G>T ENSP00000360316.3:n.877-2406G>T
ENST00000535035.5:c.610-2406G>T ENSP00000440191.2:n.610-2406G>T
NM_014762.3:c.877-2406G>T NP_055577.1:n.877-2406G>T
NM_014762.4:c.877-2406G>T MANE Select NP_055577.1:n.877-2406G>T