Canonical Allele Identifier: CA359499156

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37125432G>C (hg19) ; chr5:g.37125330G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37125330G>C , CM000667.2:g.37125330G>C	GRCh38
NC_000005.9:g.37125432G>C , CM000667.1:g.37125432G>C	GRCh37
NC_000005.8:g.37161189G>C	NCBI36
NG_032772.1:g.129099C>G
NG_032772.2:g.129099C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000510830.2:n.1871C>G
ENST00000651892.2:c.8872C>G MANE Select	ENSP00000498265.2:p.Arg2958Gly
ENST00000676160.1:n.733C>G
ENST00000425232.6:c.8710C>G	ENSP00000389014.2:p.Arg2904Gly
ENST00000508244.5:c.8710C>G	ENSP00000421690.1:p.Arg2904Gly
ENST00000509849.5:c.5884C>G	ENSP00000426337.1:n.5884C>G
ENST00000509957.5:n.4053C>G
ENST00000512288.5:n.342-3546C>G
ENST00000514429.5:c.5908C>G	ENSP00000424223.1:p.Arg1970Gly
NM_023073.3:c.8710C>G	NP_075561.3:p.Arg2904Gly
XM_005248345.2:c.8872C>G	XP_005248402.1:p.Arg2958Gly
XM_005248346.2:c.8869C>G	XP_005248403.1:p.Arg2957Gly
XM_005248347.2:c.8869C>G	XP_005248404.1:p.Arg2957Gly
XM_005248349.2:c.8761C>G	XP_005248406.1:p.Arg2921Gly
XM_005248350.2:c.8743C>G	XP_005248407.1:p.Arg2915Gly
XM_005248353.3:c.5515C>G	XP_005248410.1:p.Arg1839Gly
XM_006714489.2:c.8872C>G	XP_006714552.1:p.Arg2958Gly
XM_006714491.2:c.3445C>G	XP_006714554.1:p.Arg1149Gly
XM_011514085.1:c.8872C>G	XP_011512387.1:p.Arg2958Gly
XM_011514086.1:c.8872C>G	XP_011512388.1:p.Arg2958Gly
XM_011514087.1:c.8818C>G	XP_011512389.1:p.Arg2940Gly
XM_011514088.1:c.8764C>G	XP_011512390.1:p.Arg2922Gly
XM_011514089.1:c.8872C>G	XP_011512391.1:p.Arg2958Gly
XM_011514090.1:c.8554C>G	XP_011512392.1:p.Arg2852Gly
XM_011514091.1:c.8200C>G	XP_011512393.1:p.Arg2734Gly
XM_011514092.1:c.8872C>G	XP_011512394.1:p.Arg2958Gly
XM_011514094.1:c.6097C>G	XP_011512396.1:p.Arg2033Gly
XR_427661.2:n.9047C>G
XR_925644.1:n.9047C>G
XM_005248345.4:c.8872C>G	XP_005248402.1:p.Arg2958Gly
XM_005248346.4:c.8869C>G	XP_005248403.1:p.Arg2957Gly
XM_005248347.4:c.8869C>G	XP_005248404.1:p.Arg2957Gly
XM_005248349.4:c.8761C>G	XP_005248406.1:p.Arg2921Gly
XM_005248350.4:c.8743C>G	XP_005248407.1:p.Arg2915Gly
XM_006714491.3:c.3445C>G	XP_006714554.1:p.Arg1149Gly
XM_011514085.3:c.8872C>G	XP_011512387.1:p.Arg2958Gly
XM_011514086.3:c.8872C>G	XP_011512388.1:p.Arg2958Gly
XM_011514087.2:c.8818C>G	XP_011512389.1:p.Arg2940Gly
XM_011514088.2:c.8764C>G	XP_011512390.1:p.Arg2922Gly
XM_011514089.2:c.8872C>G	XP_011512391.1:p.Arg2958Gly
XM_011514090.3:c.8554C>G	XP_011512392.1:p.Arg2852Gly
XM_011514092.2:c.8872C>G	XP_011512394.1:p.Arg2958Gly
XM_011514094.2:c.6097C>G	XP_011512396.1:p.Arg2033Gly
XM_017009760.1:c.8683C>G	XP_016865249.1:p.Arg2895Gly
XM_017009761.2:c.8683C>G	XP_016865250.1:p.Arg2895Gly
XM_017009763.1:c.7879C>G	XP_016865252.1:p.Arg2627Gly
XM_017009765.1:c.7684C>G	XP_016865254.1:p.Arg2562Gly
XM_017009766.1:c.5515C>G	XP_016865255.1:p.Arg1839Gly
XM_024446183.1:c.8683C>G	XP_024301951.1:p.Arg2895Gly
XM_024446184.1:c.8554C>G	XP_024301952.1:p.Arg2852Gly
XM_024446185.1:c.8200C>G	XP_024301953.1:p.Arg2734Gly
XM_024446186.1:c.7879C>G	XP_024301954.1:p.Arg2627Gly
XR_925644.2:n.9096C>G
NM_001384732.1:c.8872C>G MANE Select	NP_001371661.1:p.Arg2958Gly
NM_023073.4:c.8710C>G	NP_075561.3:p.Arg2904Gly