Canonical Allele Identifier: CA2360720076
Gene: CDK5RAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33363039G>C , CM000682.2:g.33363039G>C GRCh38
NC_000020.10:g.31950845G>C , CM000682.1:g.31950845G>C GRCh37
NC_000020.9:g.31414506G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000346416.7:c.1543-2548C>G MANE Select ENSP00000217372.2:n.1543-2548C>G
ENST00000339269.5:c.1312-2548C>G ENSP00000341840.5:n.1312-2548C>G
ENST00000346416.6:c.1543-2548C>G ENSP00000217372.2:n.1543-2548C>G
ENST00000357886.8:c.1585-2548C>G ENSP00000350558.4:n.1585-2548C>G
ENST00000427097.5:c.549-2548C>G
ENST00000461710.5:n.1000-2548C>G
ENST00000473997.5:c.1273-2548C>G ENSP00000476857.1:n.1273-2548C>G
ENST00000481964.5:n.520-2548C>G
ENST00000482967.5:n.415-2548C>G
ENST00000496381.5:n.718-2548C>G
ENST00000498525.5:n.535-3952C>G
NM_001278167.1:c.1540-2548C>G NP_001265096.1:n.1540-2548C>G
NM_001278168.1:c.1312-2548C>G NP_001265097.1:n.1312-2548C>G
NM_001278169.1:c.1462-2548C>G NP_001265098.1:n.1462-2548C>G
NM_016082.4:c.1546-2548C>G NP_057166.4:n.1546-2548C>G
NM_016408.3:c.1543-2548C>G NP_057492.2:n.1543-2548C>G
XM_011528855.1:c.1231-2548C>G XP_011527157.1:n.1231-2548C>G
XM_011528856.1:c.1231-2548C>G XP_011527158.1:n.1231-2548C>G
XM_011528857.1:c.1213-2548C>G XP_011527159.1:n.1213-2548C>G
XM_011528858.1:c.1162-2548C>G XP_011527160.1:n.1162-2548C>G
XM_011528859.1:c.1162-2548C>G XP_011527161.1:n.1162-2548C>G
XM_011528860.1:c.781-2548C>G XP_011527162.1:n.781-2548C>G
XR_936548.1:n.1750-2548C>G
NM_001365728.1:c.1585-2548C>G NP_001352657.1:n.1585-2548C>G
XM_011528856.3:c.1231-2548C>G XP_011527158.1:n.1231-2548C>G
XM_011528857.2:c.1213-2548C>G XP_011527159.1:n.1213-2548C>G
XM_011528859.2:c.1162-2548C>G XP_011527161.1:n.1162-2548C>G
XM_017027876.2:c.781-2548C>G XP_016883365.1:n.781-2548C>G
XM_017027877.1:c.745-2548C>G XP_016883366.1:n.745-2548C>G
XM_024451892.1:c.994-2548C>G XP_024307660.1:n.994-2548C>G
XM_024451893.1:c.994-2548C>G XP_024307661.1:n.994-2548C>G
XM_024451894.1:c.994-2548C>G XP_024307662.1:n.994-2548C>G
XM_024451895.1:c.994-2548C>G XP_024307663.1:n.994-2548C>G
XM_024451896.1:c.781-2548C>G XP_024307664.1:n.781-2548C>G
XM_024451897.1:c.781-2548C>G XP_024307665.1:n.781-2548C>G
XR_001754289.2:n.1608-2548C>G
XR_001754290.2:n.1860-2548C>G
NM_016408.4:c.1543-2548C>G MANE Select NP_057492.2:n.1543-2548C>G
NM_001278167.2:c.1540-2548C>G NP_001265096.1:n.1540-2548C>G
NM_001278168.2:c.1312-2548C>G NP_001265097.1:n.1312-2548C>G