Canonical Allele Identifier: CA359496894

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37122565C>T (hg19) ; chr5:g.37122463C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37122463C>T , CM000667.2:g.37122463C>T	GRCh38
NC_000005.9:g.37122565C>T , CM000667.1:g.37122565C>T	GRCh37
NC_000005.8:g.37158322C>T	NCBI36
NG_032772.1:g.131966G>A
NG_032772.2:g.131966G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651892.2:c.8984G>A MANE Select	ENSP00000498265.2:p.Arg2995Lys
ENST00000676160.1:n.845G>A
ENST00000425232.6:c.8822G>A	ENSP00000389014.2:p.Arg2941Lys
ENST00000508244.5:c.8822G>A	ENSP00000421690.1:p.Arg2941Lys
ENST00000509849.5:c.5996G>A	ENSP00000426337.1:n.5996G>A
ENST00000512288.5:n.342-679G>A
ENST00000514429.5:c.6020G>A	ENSP00000424223.1:p.Arg2007Lys
NM_023073.3:c.8822G>A	NP_075561.3:p.Arg2941Lys
XM_005248345.2:c.8984G>A	XP_005248402.1:p.Arg2995Lys
XM_005248346.2:c.8981G>A	XP_005248403.1:p.Arg2994Lys
XM_005248347.2:c.8981G>A	XP_005248404.1:p.Arg2994Lys
XM_005248349.2:c.8873G>A	XP_005248406.1:p.Arg2958Lys
XM_005248350.2:c.8855G>A	XP_005248407.1:p.Arg2952Lys
XM_005248353.3:c.5627G>A	XP_005248410.1:p.Arg1876Lys
XM_006714489.2:c.8984G>A	XP_006714552.1:p.Arg2995Lys
XM_006714491.2:c.3557G>A	XP_006714554.1:p.Arg1186Lys
XM_011514085.1:c.8984G>A	XP_011512387.1:p.Arg2995Lys
XM_011514086.1:c.8984G>A	XP_011512388.1:p.Arg2995Lys
XM_011514087.1:c.8930G>A	XP_011512389.1:p.Arg2977Lys
XM_011514088.1:c.8876G>A	XP_011512390.1:p.Arg2959Lys
XM_011514089.1:c.8984G>A	XP_011512391.1:p.Arg2995Lys
XM_011514090.1:c.8666G>A	XP_011512392.1:p.Arg2889Lys
XM_011514091.1:c.8312G>A	XP_011512393.1:p.Arg2771Lys
XM_011514092.1:c.8984G>A	XP_011512394.1:p.Arg2995Lys
XM_011514094.1:c.6209G>A	XP_011512396.1:p.Arg2070Lys
XR_427661.2:n.9159G>A
XR_925644.1:n.9159G>A
XM_005248345.4:c.8984G>A	XP_005248402.1:p.Arg2995Lys
XM_005248346.4:c.8981G>A	XP_005248403.1:p.Arg2994Lys
XM_005248347.4:c.8981G>A	XP_005248404.1:p.Arg2994Lys
XM_005248349.4:c.8873G>A	XP_005248406.1:p.Arg2958Lys
XM_005248350.4:c.8855G>A	XP_005248407.1:p.Arg2952Lys
XM_006714491.3:c.3557G>A	XP_006714554.1:p.Arg1186Lys
XM_011514085.3:c.8984G>A	XP_011512387.1:p.Arg2995Lys
XM_011514086.3:c.8984G>A	XP_011512388.1:p.Arg2995Lys
XM_011514087.2:c.8930G>A	XP_011512389.1:p.Arg2977Lys
XM_011514088.2:c.8876G>A	XP_011512390.1:p.Arg2959Lys
XM_011514089.2:c.8984G>A	XP_011512391.1:p.Arg2995Lys
XM_011514090.3:c.8666G>A	XP_011512392.1:p.Arg2889Lys
XM_011514092.2:c.8984G>A	XP_011512394.1:p.Arg2995Lys
XM_011514094.2:c.6209G>A	XP_011512396.1:p.Arg2070Lys
XM_017009760.1:c.8795G>A	XP_016865249.1:p.Arg2932Lys
XM_017009761.2:c.8795G>A	XP_016865250.1:p.Arg2932Lys
XM_017009763.1:c.7991G>A	XP_016865252.1:p.Arg2664Lys
XM_017009765.1:c.7796G>A	XP_016865254.1:p.Arg2599Lys
XM_017009766.1:c.5627G>A	XP_016865255.1:p.Arg1876Lys
XM_024446183.1:c.8795G>A	XP_024301951.1:p.Arg2932Lys
XM_024446184.1:c.8666G>A	XP_024301952.1:p.Arg2889Lys
XM_024446185.1:c.8312G>A	XP_024301953.1:p.Arg2771Lys
XM_024446186.1:c.7991G>A	XP_024301954.1:p.Arg2664Lys
XR_925644.2:n.9208G>A
NM_001384732.1:c.8984G>A MANE Select	NP_001371661.1:p.Arg2995Lys
NM_023073.4:c.8822G>A	NP_075561.3:p.Arg2941Lys