Canonical Allele Identifier: CA359498404

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37125359G>T (hg19) ; chr5:g.37125257G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37125257G>T , CM000667.2:g.37125257G>T	GRCh38
NC_000005.9:g.37125359G>T , CM000667.1:g.37125359G>T	GRCh37
NC_000005.8:g.37161116G>T	NCBI36
NG_032772.1:g.129172C>A
NG_032772.2:g.129172C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000510830.2:n.1944C>A
ENST00000651892.2:c.8945C>A MANE Select	ENSP00000498265.2:p.Pro2982His
ENST00000676160.1:n.806C>A
ENST00000425232.6:c.8783C>A	ENSP00000389014.2:p.Pro2928His
ENST00000508244.5:c.8783C>A	ENSP00000421690.1:p.Pro2928His
ENST00000509849.5:c.5957C>A	ENSP00000426337.1:n.5957C>A
ENST00000509957.5:n.4126C>A
ENST00000512288.5:n.342-3473C>A
ENST00000514429.5:c.5981C>A	ENSP00000424223.1:p.Pro1994His
NM_023073.3:c.8783C>A	NP_075561.3:p.Pro2928His
XM_005248345.2:c.8945C>A	XP_005248402.1:p.Pro2982His
XM_005248346.2:c.8942C>A	XP_005248403.1:p.Pro2981His
XM_005248347.2:c.8942C>A	XP_005248404.1:p.Pro2981His
XM_005248349.2:c.8834C>A	XP_005248406.1:p.Pro2945His
XM_005248350.2:c.8816C>A	XP_005248407.1:p.Pro2939His
XM_005248353.3:c.5588C>A	XP_005248410.1:p.Pro1863His
XM_006714489.2:c.8945C>A	XP_006714552.1:p.Pro2982His
XM_006714491.2:c.3518C>A	XP_006714554.1:p.Pro1173His
XM_011514085.1:c.8945C>A	XP_011512387.1:p.Pro2982His
XM_011514086.1:c.8945C>A	XP_011512388.1:p.Pro2982His
XM_011514087.1:c.8891C>A	XP_011512389.1:p.Pro2964His
XM_011514088.1:c.8837C>A	XP_011512390.1:p.Pro2946His
XM_011514089.1:c.8945C>A	XP_011512391.1:p.Pro2982His
XM_011514090.1:c.8627C>A	XP_011512392.1:p.Pro2876His
XM_011514091.1:c.8273C>A	XP_011512393.1:p.Pro2758His
XM_011514092.1:c.8945C>A	XP_011512394.1:p.Pro2982His
XM_011514094.1:c.6170C>A	XP_011512396.1:p.Pro2057His
XR_427661.2:n.9120C>A
XR_925644.1:n.9120C>A
XM_005248345.4:c.8945C>A	XP_005248402.1:p.Pro2982His
XM_005248346.4:c.8942C>A	XP_005248403.1:p.Pro2981His
XM_005248347.4:c.8942C>A	XP_005248404.1:p.Pro2981His
XM_005248349.4:c.8834C>A	XP_005248406.1:p.Pro2945His
XM_005248350.4:c.8816C>A	XP_005248407.1:p.Pro2939His
XM_006714491.3:c.3518C>A	XP_006714554.1:p.Pro1173His
XM_011514085.3:c.8945C>A	XP_011512387.1:p.Pro2982His
XM_011514086.3:c.8945C>A	XP_011512388.1:p.Pro2982His
XM_011514087.2:c.8891C>A	XP_011512389.1:p.Pro2964His
XM_011514088.2:c.8837C>A	XP_011512390.1:p.Pro2946His
XM_011514089.2:c.8945C>A	XP_011512391.1:p.Pro2982His
XM_011514090.3:c.8627C>A	XP_011512392.1:p.Pro2876His
XM_011514092.2:c.8945C>A	XP_011512394.1:p.Pro2982His
XM_011514094.2:c.6170C>A	XP_011512396.1:p.Pro2057His
XM_017009760.1:c.8756C>A	XP_016865249.1:p.Pro2919His
XM_017009761.2:c.8756C>A	XP_016865250.1:p.Pro2919His
XM_017009763.1:c.7952C>A	XP_016865252.1:p.Pro2651His
XM_017009765.1:c.7757C>A	XP_016865254.1:p.Pro2586His
XM_017009766.1:c.5588C>A	XP_016865255.1:p.Pro1863His
XM_024446183.1:c.8756C>A	XP_024301951.1:p.Pro2919His
XM_024446184.1:c.8627C>A	XP_024301952.1:p.Pro2876His
XM_024446185.1:c.8273C>A	XP_024301953.1:p.Pro2758His
XM_024446186.1:c.7952C>A	XP_024301954.1:p.Pro2651His
XR_925644.2:n.9169C>A
NM_001384732.1:c.8945C>A MANE Select	NP_001371661.1:p.Pro2982His
NM_023073.4:c.8783C>A	NP_075561.3:p.Pro2928His