Canonical Allele Identifier: CA117071219

Gene: CPLANE1 CPLANE1-AS1

Linked Data

• dbSNP Id: rs892698217
• gnomAD v2: 5-37249456-A-T
• gnomAD v3: 5-37249354-A-T
• gnomAD v4: 5-37249354-A-T
• MyVariant Identifiers: chr5:g.37249456A>T (hg19) ; chr5:g.37249354A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37249354A>T , CM000667.2:g.37249354A>T	GRCh38
NC_000005.9:g.37249456A>T , CM000667.1:g.37249456A>T	GRCh37
NC_000005.8:g.37285213A>T	NCBI36
NG_032772.1:g.5075T>A
NG_032772.2:g.5075T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651892.2:c.-157T>A (CPLANE1) MANE Select	ENSP00000498265.2:n.-157T>A
ENST00000675547.1:n.12T>A (CPLANE1)
ENST00000425232.6:c.-157T>A (CPLANE1)	ENSP00000389014.2:n.-157T>A
NM_023073.3:c.-157T>A (CPLANE1)	NP_075561.3:n.-157T>A
XM_005248345.2:c.-157T>A (CPLANE1)	XP_005248402.1:n.-157T>A
XM_005248346.2:c.-157T>A (CPLANE1)	XP_005248403.1:n.-157T>A
XM_005248347.2:c.-157T>A (CPLANE1)	XP_005248404.1:n.-157T>A
XM_005248349.2:c.-157T>A (CPLANE1)	XP_005248406.1:n.-157T>A
XM_005248350.2:c.-157T>A (CPLANE1)	XP_005248407.1:n.-157T>A
XM_006714489.2:c.-157T>A (CPLANE1)	XP_006714552.1:n.-157T>A
XM_011514086.1:c.-200T>A (CPLANE1)	XP_011512388.1:n.-200T>A
XM_011514087.1:c.-157T>A (CPLANE1)	XP_011512389.1:n.-157T>A
XM_011514088.1:c.-157T>A (CPLANE1)	XP_011512390.1:n.-157T>A
XM_011514089.1:c.-157T>A (CPLANE1)	XP_011512391.1:n.-157T>A
XM_011514090.1:c.-394T>A (CPLANE1)	XP_011512392.1:n.-394T>A
XM_011514092.1:c.-157T>A (CPLANE1)	XP_011512394.1:n.-157T>A
XM_011514093.1:c.-157T>A (CPLANE1)	XP_011512395.1:n.-157T>A
XR_427661.2:n.19T>A (CPLANE1)
XR_925644.1:n.19T>A (CPLANE1)
XR_925921.1:n.171+133A>T (CPLANE1-AS1)
NR_134263.1:n.176+133A>T (CPLANE1-AS1)
XM_005248345.4:c.-157T>A (CPLANE1)	XP_005248402.1:n.-157T>A
XM_005248346.4:c.-157T>A (CPLANE1)	XP_005248403.1:n.-157T>A
XM_005248347.4:c.-157T>A (CPLANE1)	XP_005248404.1:n.-157T>A
XM_005248349.4:c.-157T>A (CPLANE1)	XP_005248406.1:n.-157T>A
XM_005248350.4:c.-157T>A (CPLANE1)	XP_005248407.1:n.-157T>A
XM_011514086.3:c.-200T>A (CPLANE1)	XP_011512388.1:n.-200T>A
XM_011514087.2:c.-157T>A (CPLANE1)	XP_011512389.1:n.-157T>A
XM_011514088.2:c.-157T>A (CPLANE1)	XP_011512390.1:n.-157T>A
XM_011514089.2:c.-157T>A (CPLANE1)	XP_011512391.1:n.-157T>A
XM_011514090.3:c.-394T>A (CPLANE1)	XP_011512392.1:n.-394T>A
XM_011514092.2:c.-157T>A (CPLANE1)	XP_011512394.1:n.-157T>A
XM_017009761.2:c.-129T>A (CPLANE1)	XP_016865250.1:n.-129T>A
XM_017009765.1:c.-1088T>A (CPLANE1)	XP_016865254.1:n.-1088T>A
XM_024446184.1:c.-437T>A (CPLANE1)	XP_024301952.1:n.-437T>A
XM_024446185.1:c.-684T>A (CPLANE1)	XP_024301953.1:n.-684T>A
XM_024446186.1:c.-1155T>A (CPLANE1)	XP_024301954.1:n.-1155T>A
XR_001742208.1:n.68T>A (CPLANE1)
XR_002956171.1:n.68T>A (CPLANE1)
XR_925644.2:n.68T>A (CPLANE1)
NM_001384732.1:c.-157T>A (CPLANE1) MANE Select	NP_001371661.1:n.-157T>A
NM_023073.4:c.-157T>A (CPLANE1)	NP_075561.3:n.-157T>A