Canonical Allele Identifier: CA359491926

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37115116C>G (hg19) ; chr5:g.37115014C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37115014C>G , CM000667.2:g.37115014C>G	GRCh38
NC_000005.9:g.37115116C>G , CM000667.1:g.37115116C>G	GRCh37
NC_000005.8:g.37150873C>G	NCBI36
NG_032772.1:g.139415G>C
NG_032772.2:g.139415G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651892.2:c.9346G>C MANE Select	ENSP00000498265.2:p.Gly3116Arg
ENST00000676160.1:n.1852G>C
ENST00000425232.6:c.9184G>C	ENSP00000389014.2:p.Gly3062Arg
ENST00000508244.5:c.9184G>C	ENSP00000421690.1:p.Gly3062Arg
ENST00000509849.5:c.6358G>C	ENSP00000426337.1:n.6358G>C
ENST00000514429.5:c.6382G>C	ENSP00000424223.1:p.Gly2128Arg
NM_023073.3:c.9184G>C	NP_075561.3:p.Gly3062Arg
XM_005248345.2:c.9346G>C	XP_005248402.1:p.Gly3116Arg
XM_005248346.2:c.9343G>C	XP_005248403.1:p.Gly3115Arg
XM_005248347.2:c.9343G>C	XP_005248404.1:p.Gly3115Arg
XM_005248349.2:c.9235G>C	XP_005248406.1:p.Gly3079Arg
XM_005248350.2:c.9217G>C	XP_005248407.1:p.Gly3073Arg
XM_005248353.3:c.5989G>C	XP_005248410.1:p.Gly1997Arg
XM_006714489.2:c.9346G>C	XP_006714552.1:p.Gly3116Arg
XM_006714491.2:c.3919G>C	XP_006714554.1:p.Gly1307Arg
XM_011514085.1:c.9346G>C	XP_011512387.1:p.Gly3116Arg
XM_011514086.1:c.9346G>C	XP_011512388.1:p.Gly3116Arg
XM_011514087.1:c.9292G>C	XP_011512389.1:p.Gly3098Arg
XM_011514088.1:c.9238G>C	XP_011512390.1:p.Gly3080Arg
XM_011514089.1:c.9346G>C	XP_011512391.1:p.Gly3116Arg
XM_011514090.1:c.9028G>C	XP_011512392.1:p.Gly3010Arg
XM_011514091.1:c.8674G>C	XP_011512393.1:p.Gly2892Arg
XM_011514094.1:c.6571G>C	XP_011512396.1:p.Gly2191Arg
XR_427661.2:n.9521G>C
XR_925644.1:n.9521G>C
XM_005248345.4:c.9346G>C	XP_005248402.1:p.Gly3116Arg
XM_005248346.4:c.9343G>C	XP_005248403.1:p.Gly3115Arg
XM_005248347.4:c.9343G>C	XP_005248404.1:p.Gly3115Arg
XM_005248349.4:c.9235G>C	XP_005248406.1:p.Gly3079Arg
XM_005248350.4:c.9217G>C	XP_005248407.1:p.Gly3073Arg
XM_006714491.3:c.3919G>C	XP_006714554.1:p.Gly1307Arg
XM_011514085.3:c.9346G>C	XP_011512387.1:p.Gly3116Arg
XM_011514086.3:c.9346G>C	XP_011512388.1:p.Gly3116Arg
XM_011514087.2:c.9292G>C	XP_011512389.1:p.Gly3098Arg
XM_011514088.2:c.9238G>C	XP_011512390.1:p.Gly3080Arg
XM_011514089.2:c.9346G>C	XP_011512391.1:p.Gly3116Arg
XM_011514090.3:c.9028G>C	XP_011512392.1:p.Gly3010Arg
XM_011514094.2:c.6571G>C	XP_011512396.1:p.Gly2191Arg
XM_017009760.1:c.9157G>C	XP_016865249.1:p.Gly3053Arg
XM_017009761.2:c.9157G>C	XP_016865250.1:p.Gly3053Arg
XM_017009763.1:c.8353G>C	XP_016865252.1:p.Gly2785Arg
XM_017009765.1:c.8158G>C	XP_016865254.1:p.Gly2720Arg
XM_017009766.1:c.5989G>C	XP_016865255.1:p.Gly1997Arg
XM_024446183.1:c.9157G>C	XP_024301951.1:p.Gly3053Arg
XM_024446184.1:c.9028G>C	XP_024301952.1:p.Gly3010Arg
XM_024446185.1:c.8674G>C	XP_024301953.1:p.Gly2892Arg
XM_024446186.1:c.8353G>C	XP_024301954.1:p.Gly2785Arg
XR_925644.2:n.9570G>C
NM_001384732.1:c.9346G>C MANE Select	NP_001371661.1:p.Gly3116Arg
NM_023073.4:c.9184G>C	NP_075561.3:p.Gly3062Arg