Canonical Allele Identifier: CA359476397

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37165709T>C (hg19) ; chr5:g.37165607T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37165607T>C , CM000667.2:g.37165607T>C	GRCh38
NC_000005.9:g.37165709T>C , CM000667.1:g.37165709T>C	GRCh37
NC_000005.8:g.37201466T>C	NCBI36
NG_032772.1:g.88822A>G
NG_032772.2:g.88822A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000651892.2:c.7465A>G MANE Select	ENSP00000498265.2:p.Asn2489Asp
ENST00000675149.1:n.585A>G
ENST00000425232.6:c.7465A>G	ENSP00000389014.2:p.Asn2489Asp
ENST00000508244.5:c.7465A>G	ENSP00000421690.1:p.Asn2489Asp
ENST00000509849.5:c.4477A>G	ENSP00000426337.1:p.Asn1493Asp
ENST00000511824.2:c.537A>G
ENST00000514429.5:c.4609A>G	ENSP00000424223.1:p.Asn1537Asp
NM_023073.3:c.7465A>G	NP_075561.3:p.Asn2489Asp
XM_005248345.2:c.7465A>G	XP_005248402.1:p.Asn2489Asp
XM_005248346.2:c.7462A>G	XP_005248403.1:p.Asn2488Asp
XM_005248347.2:c.7462A>G	XP_005248404.1:p.Asn2488Asp
XM_005248349.2:c.7462A>G	XP_005248406.1:p.Asn2488Asp
XM_005248350.2:c.7336A>G	XP_005248407.1:p.Asn2446Asp
XM_005248353.3:c.4108A>G	XP_005248410.1:p.Asn1370Asp
XM_006714489.2:c.7465A>G	XP_006714552.1:p.Asn2489Asp
XM_006714491.2:c.2038A>G	XP_006714554.1:p.Asn680Asp
XM_011514085.1:c.7465A>G	XP_011512387.1:p.Asn2489Asp
XM_011514086.1:c.7465A>G	XP_011512388.1:p.Asn2489Asp
XM_011514087.1:c.7465A>G	XP_011512389.1:p.Asn2489Asp
XM_011514088.1:c.7465A>G	XP_011512390.1:p.Asn2489Asp
XM_011514089.1:c.7465A>G	XP_011512391.1:p.Asn2489Asp
XM_011514090.1:c.7147A>G	XP_011512392.1:p.Asn2383Asp
XM_011514091.1:c.6793A>G	XP_011512393.1:p.Asn2265Asp
XM_011514092.1:c.7465A>G	XP_011512394.1:p.Asn2489Asp
XM_011514093.1:c.7465A>G	XP_011512395.1:p.Asn2489Asp
XM_011514094.1:c.4690A>G	XP_011512396.1:p.Asn1564Asp
XR_427661.2:n.7640A>G
XR_925644.1:n.7640A>G
XM_005248345.4:c.7465A>G	XP_005248402.1:p.Asn2489Asp
XM_005248346.4:c.7462A>G	XP_005248403.1:p.Asn2488Asp
XM_005248347.4:c.7462A>G	XP_005248404.1:p.Asn2488Asp
XM_005248349.4:c.7462A>G	XP_005248406.1:p.Asn2488Asp
XM_005248350.4:c.7336A>G	XP_005248407.1:p.Asn2446Asp
XM_006714491.3:c.2038A>G	XP_006714554.1:p.Asn680Asp
XM_011514085.3:c.7465A>G	XP_011512387.1:p.Asn2489Asp
XM_011514086.3:c.7465A>G	XP_011512388.1:p.Asn2489Asp
XM_011514087.2:c.7465A>G	XP_011512389.1:p.Asn2489Asp
XM_011514088.2:c.7465A>G	XP_011512390.1:p.Asn2489Asp
XM_011514089.2:c.7465A>G	XP_011512391.1:p.Asn2489Asp
XM_011514090.3:c.7147A>G	XP_011512392.1:p.Asn2383Asp
XM_011514092.2:c.7465A>G	XP_011512394.1:p.Asn2489Asp
XM_011514094.2:c.4690A>G	XP_011512396.1:p.Asn1564Asp
XM_017009760.1:c.7276A>G	XP_016865249.1:p.Asn2426Asp
XM_017009761.2:c.7276A>G	XP_016865250.1:p.Asn2426Asp
XM_017009763.1:c.6472A>G	XP_016865252.1:p.Asn2158Asp
XM_017009765.1:c.6277A>G	XP_016865254.1:p.Asn2093Asp
XM_017009766.1:c.4108A>G	XP_016865255.1:p.Asn1370Asp
XM_024446183.1:c.7276A>G	XP_024301951.1:p.Asn2426Asp
XM_024446184.1:c.7147A>G	XP_024301952.1:p.Asn2383Asp
XM_024446185.1:c.6793A>G	XP_024301953.1:p.Asn2265Asp
XM_024446186.1:c.6472A>G	XP_024301954.1:p.Asn2158Asp
XR_001742208.1:n.7689A>G
XR_002956171.1:n.7689A>G
XR_925644.2:n.7689A>G
NM_001384732.1:c.7465A>G MANE Select	NP_001371661.1:p.Asn2489Asp
NM_023073.4:c.7465A>G	NP_075561.3:p.Asn2489Asp