Canonical Allele Identifier: CA359497046

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37122580G>C (hg19) ; chr5:g.37122478G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37122478G>C , CM000667.2:g.37122478G>C	GRCh38
NC_000005.9:g.37122580G>C , CM000667.1:g.37122580G>C	GRCh37
NC_000005.8:g.37158337G>C	NCBI36
NG_032772.1:g.131951C>G
NG_032772.2:g.131951C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651892.2:c.8969C>G MANE Select	ENSP00000498265.2:p.Thr2990Ser
ENST00000676160.1:n.830C>G
ENST00000425232.6:c.8807C>G	ENSP00000389014.2:p.Thr2936Ser
ENST00000508244.5:c.8807C>G	ENSP00000421690.1:p.Thr2936Ser
ENST00000509849.5:c.5981C>G	ENSP00000426337.1:n.5981C>G
ENST00000512288.5:n.342-694C>G
ENST00000514429.5:c.6005C>G	ENSP00000424223.1:p.Thr2002Ser
NM_023073.3:c.8807C>G	NP_075561.3:p.Thr2936Ser
XM_005248345.2:c.8969C>G	XP_005248402.1:p.Thr2990Ser
XM_005248346.2:c.8966C>G	XP_005248403.1:p.Thr2989Ser
XM_005248347.2:c.8966C>G	XP_005248404.1:p.Thr2989Ser
XM_005248349.2:c.8858C>G	XP_005248406.1:p.Thr2953Ser
XM_005248350.2:c.8840C>G	XP_005248407.1:p.Thr2947Ser
XM_005248353.3:c.5612C>G	XP_005248410.1:p.Thr1871Ser
XM_006714489.2:c.8969C>G	XP_006714552.1:p.Thr2990Ser
XM_006714491.2:c.3542C>G	XP_006714554.1:p.Thr1181Ser
XM_011514085.1:c.8969C>G	XP_011512387.1:p.Thr2990Ser
XM_011514086.1:c.8969C>G	XP_011512388.1:p.Thr2990Ser
XM_011514087.1:c.8915C>G	XP_011512389.1:p.Thr2972Ser
XM_011514088.1:c.8861C>G	XP_011512390.1:p.Thr2954Ser
XM_011514089.1:c.8969C>G	XP_011512391.1:p.Thr2990Ser
XM_011514090.1:c.8651C>G	XP_011512392.1:p.Thr2884Ser
XM_011514091.1:c.8297C>G	XP_011512393.1:p.Thr2766Ser
XM_011514092.1:c.8969C>G	XP_011512394.1:p.Thr2990Ser
XM_011514094.1:c.6194C>G	XP_011512396.1:p.Thr2065Ser
XR_427661.2:n.9144C>G
XR_925644.1:n.9144C>G
XM_005248345.4:c.8969C>G	XP_005248402.1:p.Thr2990Ser
XM_005248346.4:c.8966C>G	XP_005248403.1:p.Thr2989Ser
XM_005248347.4:c.8966C>G	XP_005248404.1:p.Thr2989Ser
XM_005248349.4:c.8858C>G	XP_005248406.1:p.Thr2953Ser
XM_005248350.4:c.8840C>G	XP_005248407.1:p.Thr2947Ser
XM_006714491.3:c.3542C>G	XP_006714554.1:p.Thr1181Ser
XM_011514085.3:c.8969C>G	XP_011512387.1:p.Thr2990Ser
XM_011514086.3:c.8969C>G	XP_011512388.1:p.Thr2990Ser
XM_011514087.2:c.8915C>G	XP_011512389.1:p.Thr2972Ser
XM_011514088.2:c.8861C>G	XP_011512390.1:p.Thr2954Ser
XM_011514089.2:c.8969C>G	XP_011512391.1:p.Thr2990Ser
XM_011514090.3:c.8651C>G	XP_011512392.1:p.Thr2884Ser
XM_011514092.2:c.8969C>G	XP_011512394.1:p.Thr2990Ser
XM_011514094.2:c.6194C>G	XP_011512396.1:p.Thr2065Ser
XM_017009760.1:c.8780C>G	XP_016865249.1:p.Thr2927Ser
XM_017009761.2:c.8780C>G	XP_016865250.1:p.Thr2927Ser
XM_017009763.1:c.7976C>G	XP_016865252.1:p.Thr2659Ser
XM_017009765.1:c.7781C>G	XP_016865254.1:p.Thr2594Ser
XM_017009766.1:c.5612C>G	XP_016865255.1:p.Thr1871Ser
XM_024446183.1:c.8780C>G	XP_024301951.1:p.Thr2927Ser
XM_024446184.1:c.8651C>G	XP_024301952.1:p.Thr2884Ser
XM_024446185.1:c.8297C>G	XP_024301953.1:p.Thr2766Ser
XM_024446186.1:c.7976C>G	XP_024301954.1:p.Thr2659Ser
XR_925644.2:n.9193C>G
NM_001384732.1:c.8969C>G MANE Select	NP_001371661.1:p.Thr2990Ser
NM_023073.4:c.8807C>G	NP_075561.3:p.Thr2936Ser