Canonical Allele Identifier: CA359474372

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37154074C>A (hg19) ; chr5:g.37153972C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153972C>A , CM000667.2:g.37153972C>A	GRCh38
NC_000005.9:g.37154074C>A , CM000667.1:g.37154074C>A	GRCh37
NC_000005.8:g.37189831C>A	NCBI36
NG_032772.1:g.100457G>T
NG_032772.2:g.100457G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1140G>T
ENST00000651892.2:c.8141G>T MANE Select	ENSP00000498265.2:p.Arg2714Leu
ENST00000425232.6:c.7979G>T	ENSP00000389014.2:p.Arg2660Leu
ENST00000508244.5:c.7979G>T	ENSP00000421690.1:p.Arg2660Leu
ENST00000509849.5:c.5153G>T	ENSP00000426337.1:p.Arg1718Leu
ENST00000509957.5:n.383G>T
ENST00000511210.5:n.432G>T
ENST00000511824.2:c.1255G>T
ENST00000514429.5:c.5177G>T	ENSP00000424223.1:p.Arg1726Leu
ENST00000515380.1:n.393G>T
NM_023073.3:c.7979G>T	NP_075561.3:p.Arg2660Leu
XM_005248345.2:c.8141G>T	XP_005248402.1:p.Arg2714Leu
XM_005248346.2:c.8138G>T	XP_005248403.1:p.Arg2713Leu
XM_005248347.2:c.8138G>T	XP_005248404.1:p.Arg2713Leu
XM_005248349.2:c.8030G>T	XP_005248406.1:p.Arg2677Leu
XM_005248350.2:c.8012G>T	XP_005248407.1:p.Arg2671Leu
XM_005248353.3:c.4784G>T	XP_005248410.1:p.Arg1595Leu
XM_006714489.2:c.8141G>T	XP_006714552.1:p.Arg2714Leu
XM_006714491.2:c.2714G>T	XP_006714554.1:p.Arg905Leu
XM_011514085.1:c.8141G>T	XP_011512387.1:p.Arg2714Leu
XM_011514086.1:c.8141G>T	XP_011512388.1:p.Arg2714Leu
XM_011514087.1:c.8087G>T	XP_011512389.1:p.Arg2696Leu
XM_011514088.1:c.8033G>T	XP_011512390.1:p.Arg2678Leu
XM_011514089.1:c.8141G>T	XP_011512391.1:p.Arg2714Leu
XM_011514090.1:c.7823G>T	XP_011512392.1:p.Arg2608Leu
XM_011514091.1:c.7469G>T	XP_011512393.1:p.Arg2490Leu
XM_011514092.1:c.8141G>T	XP_011512394.1:p.Arg2714Leu
XM_011514094.1:c.5366G>T	XP_011512396.1:p.Arg1789Leu
XR_427661.2:n.8316G>T
XR_925644.1:n.8316G>T
XM_005248345.4:c.8141G>T	XP_005248402.1:p.Arg2714Leu
XM_005248346.4:c.8138G>T	XP_005248403.1:p.Arg2713Leu
XM_005248347.4:c.8138G>T	XP_005248404.1:p.Arg2713Leu
XM_005248349.4:c.8030G>T	XP_005248406.1:p.Arg2677Leu
XM_005248350.4:c.8012G>T	XP_005248407.1:p.Arg2671Leu
XM_006714491.3:c.2714G>T	XP_006714554.1:p.Arg905Leu
XM_011514085.3:c.8141G>T	XP_011512387.1:p.Arg2714Leu
XM_011514086.3:c.8141G>T	XP_011512388.1:p.Arg2714Leu
XM_011514087.2:c.8087G>T	XP_011512389.1:p.Arg2696Leu
XM_011514088.2:c.8033G>T	XP_011512390.1:p.Arg2678Leu
XM_011514089.2:c.8141G>T	XP_011512391.1:p.Arg2714Leu
XM_011514090.3:c.7823G>T	XP_011512392.1:p.Arg2608Leu
XM_011514092.2:c.8141G>T	XP_011512394.1:p.Arg2714Leu
XM_011514094.2:c.5366G>T	XP_011512396.1:p.Arg1789Leu
XM_017009760.1:c.7952G>T	XP_016865249.1:p.Arg2651Leu
XM_017009761.2:c.7952G>T	XP_016865250.1:p.Arg2651Leu
XM_017009763.1:c.7148G>T	XP_016865252.1:p.Arg2383Leu
XM_017009765.1:c.6953G>T	XP_016865254.1:p.Arg2318Leu
XM_017009766.1:c.4784G>T	XP_016865255.1:p.Arg1595Leu
XM_024446183.1:c.7952G>T	XP_024301951.1:p.Arg2651Leu
XM_024446184.1:c.7823G>T	XP_024301952.1:p.Arg2608Leu
XM_024446185.1:c.7469G>T	XP_024301953.1:p.Arg2490Leu
XM_024446186.1:c.7148G>T	XP_024301954.1:p.Arg2383Leu
XR_001742208.1:n.8310G>T
XR_002956171.1:n.8256G>T
XR_925644.2:n.8365G>T
NM_001384732.1:c.8141G>T MANE Select	NP_001371661.1:p.Arg2714Leu
NM_023073.4:c.7979G>T	NP_075561.3:p.Arg2660Leu