Canonical Allele Identifier: CA810319217

Gene: CPLANE1 CPLANE1-AS1

Linked Data

• dbSNP Id: rs1325882947
• gnomAD v3: 5-37249288-A-G
• gnomAD v4: 5-37249288-A-G
• MyVariant Identifiers: chr5:g.37249390A>G (hg19) ; chr5:g.37249288A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37249288A>G , CM000667.2:g.37249288A>G	GRCh38
NC_000005.9:g.37249390A>G , CM000667.1:g.37249390A>G	GRCh37
NC_000005.8:g.37285147A>G	NCBI36
NG_032772.1:g.5141T>C
NG_032772.2:g.5141T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651892.2:c.-91T>C (CPLANE1) MANE Select	ENSP00000498265.2:n.-91T>C
ENST00000675547.1:n.78T>C (CPLANE1)
ENST00000425232.6:c.-91T>C (CPLANE1)	ENSP00000389014.2:n.-91T>C
NM_023073.3:c.-91T>C (CPLANE1)	NP_075561.3:n.-91T>C
XM_005248345.2:c.-91T>C (CPLANE1)	XP_005248402.1:n.-91T>C
XM_005248346.2:c.-91T>C (CPLANE1)	XP_005248403.1:n.-91T>C
XM_005248347.2:c.-91T>C (CPLANE1)	XP_005248404.1:n.-91T>C
XM_005248349.2:c.-91T>C (CPLANE1)	XP_005248406.1:n.-91T>C
XM_005248350.2:c.-91T>C (CPLANE1)	XP_005248407.1:n.-91T>C
XM_006714489.2:c.-91T>C (CPLANE1)	XP_006714552.1:n.-91T>C
XM_011514086.1:c.-134T>C (CPLANE1)	XP_011512388.1:n.-134T>C
XM_011514087.1:c.-91T>C (CPLANE1)	XP_011512389.1:n.-91T>C
XM_011514088.1:c.-91T>C (CPLANE1)	XP_011512390.1:n.-91T>C
XM_011514089.1:c.-91T>C (CPLANE1)	XP_011512391.1:n.-91T>C
XM_011514090.1:c.-328T>C (CPLANE1)	XP_011512392.1:n.-328T>C
XM_011514092.1:c.-91T>C (CPLANE1)	XP_011512394.1:n.-91T>C
XM_011514093.1:c.-91T>C (CPLANE1)	XP_011512395.1:n.-91T>C
XR_427661.2:n.85T>C (CPLANE1)
XR_925644.1:n.85T>C (CPLANE1)
XR_925921.1:n.171+67A>G (CPLANE1-AS1)
NR_134263.1:n.176+67A>G (CPLANE1-AS1)
XM_005248345.4:c.-91T>C (CPLANE1)	XP_005248402.1:n.-91T>C
XM_005248346.4:c.-91T>C (CPLANE1)	XP_005248403.1:n.-91T>C
XM_005248347.4:c.-91T>C (CPLANE1)	XP_005248404.1:n.-91T>C
XM_005248349.4:c.-91T>C (CPLANE1)	XP_005248406.1:n.-91T>C
XM_005248350.4:c.-91T>C (CPLANE1)	XP_005248407.1:n.-91T>C
XM_011514086.3:c.-134T>C (CPLANE1)	XP_011512388.1:n.-134T>C
XM_011514087.2:c.-91T>C (CPLANE1)	XP_011512389.1:n.-91T>C
XM_011514088.2:c.-91T>C (CPLANE1)	XP_011512390.1:n.-91T>C
XM_011514089.2:c.-91T>C (CPLANE1)	XP_011512391.1:n.-91T>C
XM_011514090.3:c.-328T>C (CPLANE1)	XP_011512392.1:n.-328T>C
XM_011514092.2:c.-91T>C (CPLANE1)	XP_011512394.1:n.-91T>C
XM_017009761.2:c.-63T>C (CPLANE1)	XP_016865250.1:n.-63T>C
XM_017009765.1:c.-1022T>C (CPLANE1)	XP_016865254.1:n.-1022T>C
XM_024446184.1:c.-371T>C (CPLANE1)	XP_024301952.1:n.-371T>C
XM_024446185.1:c.-618T>C (CPLANE1)	XP_024301953.1:n.-618T>C
XM_024446186.1:c.-1089T>C (CPLANE1)	XP_024301954.1:n.-1089T>C
XR_001742208.1:n.134T>C (CPLANE1)
XR_002956171.1:n.134T>C (CPLANE1)
XR_925644.2:n.134T>C (CPLANE1)
NM_001384732.1:c.-91T>C (CPLANE1) MANE Select	NP_001371661.1:n.-91T>C
NM_023073.4:c.-91T>C (CPLANE1)	NP_075561.3:n.-91T>C