Canonical Allele Identifier: CA374721038

Gene: CDK5RAP2

Linked Data

• MyVariant Identifiers: chr9:g.123201739G>C (hg19) ; chr9:g.120439461G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120439461G>C , CM000671.2:g.120439461G>C	GRCh38
NC_000009.11:g.123201739G>C , CM000671.1:g.123201739G>C	GRCh37
NC_000009.10:g.122241560G>C	NCBI36
NG_008999.1:g.145699C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360822.8:c.2970C>G	ENSP00000354065.4:p.Asn990Lys
ENST00000416449.6:c.3564C>G	ENSP00000400395.2:p.Asn1188Lys
ENST00000479584.2:n.1907C>G
ENST00000684780.1:n.3950C>G
ENST00000685866.1:c.*1487C>G	ENSP00000509484.1:n.*1487C>G
ENST00000686376.1:c.3740C>G	ENSP00000510021.1:n.3740C>G
ENST00000686842.1:n.7214C>G
ENST00000687279.1:c.3657C>G	ENSP00000508692.1:p.Asn1219Lys
ENST00000687311.1:n.3623C>G
ENST00000687633.1:c.3561C>G	ENSP00000510289.1:p.Asn1187Lys
ENST00000688923.1:n.3032C>G
ENST00000689688.1:c.3660C>G	ENSP00000510155.1:p.Asn1220Lys
ENST00000690646.1:c.3564C>G	ENSP00000510383.1:p.Asn1188Lys
ENST00000690814.1:c.*836C>G	ENSP00000508792.1:n.*836C>G
ENST00000691504.1:n.3554C>G
ENST00000692155.1:c.3740C>G	ENSP00000510290.1:n.3740C>G
ENST00000692746.1:n.3567C>G
ENST00000693386.1:c.3564C>G	ENSP00000510003.1:p.Asn1188Lys
ENST00000693433.1:n.3554C>G
ENST00000693714.1:n.3607C>G
ENST00000693728.1:c.3564C>G	ENSP00000510580.1:p.Asn1188Lys
ENST00000349780.9:c.3660C>G MANE Select	ENSP00000343818.4:p.Asn1220Lys
ENST00000349780.8:c.3660C>G	ENSP00000343818.4:p.Asn1220Lys
ENST00000360190.8:c.3660C>G	ENSP00000353317.4:p.Asn1220Lys
ENST00000360822.7:c.2970C>G	ENSP00000354065.4:p.Asn990Lys
ENST00000416449.5:c.1842C>G	ENSP00000400395.1:p.Asn614Lys
ENST00000425647.1:c.690C>G	ENSP00000409941.1:p.Asn230Lys
ENST00000473282.6:c.*2484C>G	ENSP00000419265.1:n.*2484C>G
ENST00000480112.5:c.*1487C>G	ENSP00000418418.1:n.*1487C>G
ENST00000483412.5:n.2968C>G
NM_001011649.2:c.3660C>G	NP_001011649.1:p.Asn1220Lys
NM_001272039.1:c.2970C>G	NP_001258968.1:p.Asn990Lys
NM_018249.5:c.3660C>G	NP_060719.4:p.Asn1220Lys
NR_073554.1:n.3929C>G
NR_073555.1:n.3852C>G
NR_073556.1:n.4059C>G
NR_073557.1:n.3932C>G
NR_073558.1:n.3929C>G
XM_006717182.1:c.3564C>G	XP_006717245.1:p.Asn1188Lys
XM_006717185.1:c.2973C>G	XP_006717248.1:p.Asn991Lys
XM_011518860.1:c.3657C>G	XP_011517162.1:p.Asn1219Lys
XM_011518861.1:c.3657C>G	XP_011517163.1:p.Asn1219Lys
XM_017014921.1:c.3561C>G	XP_016870410.1:p.Asn1187Lys
XM_017014922.1:c.2826C>G	XP_016870411.1:p.Asn942Lys
XM_017014923.1:c.2973C>G	XP_016870412.1:p.Asn991Lys
XM_017014924.1:c.1455C>G	XP_016870413.1:p.Asn485Lys
NM_018249.6:c.3660C>G MANE Select	NP_060719.4:p.Asn1220Lys
NM_001011649.3:c.3660C>G	NP_001011649.1:p.Asn1220Lys
NR_073554.2:n.3926C>G
NR_073555.2:n.3849C>G
NR_073556.2:n.4056C>G
NR_073557.2:n.3929C>G
NR_073558.2:n.3926C>G
NM_001272039.2:c.2970C>G	NP_001258968.1:p.Asn990Lys