Canonical Allele Identifier: CA810319352

Gene: CPLANE1 CPLANE1-AS1

Linked Data

• dbSNP Id: rs1168213727
• gnomAD v3: 5-37249367-T-C
• gnomAD v4: 5-37249367-T-C
• MyVariant Identifiers: chr5:g.37249469T>C (hg19) ; chr5:g.37249367T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37249367T>C , CM000667.2:g.37249367T>C	GRCh38
NC_000005.9:g.37249469T>C , CM000667.1:g.37249469T>C	GRCh37
NC_000005.8:g.37285226T>C	NCBI36
NG_032772.1:g.5062A>G
NG_032772.2:g.5062A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651892.2:c.-170A>G (CPLANE1) MANE Select	ENSP00000498265.2:n.-170A>G
ENST00000425232.6:c.-170A>G (CPLANE1)	ENSP00000389014.2:n.-170A>G
NM_023073.3:c.-170A>G (CPLANE1)	NP_075561.3:n.-170A>G
XM_005248345.2:c.-170A>G (CPLANE1)	XP_005248402.1:n.-170A>G
XM_005248346.2:c.-170A>G (CPLANE1)	XP_005248403.1:n.-170A>G
XM_005248347.2:c.-170A>G (CPLANE1)	XP_005248404.1:n.-170A>G
XM_005248349.2:c.-170A>G (CPLANE1)	XP_005248406.1:n.-170A>G
XM_005248350.2:c.-170A>G (CPLANE1)	XP_005248407.1:n.-170A>G
XM_006714489.2:c.-170A>G (CPLANE1)	XP_006714552.1:n.-170A>G
XM_011514086.1:c.-213A>G (CPLANE1)	XP_011512388.1:n.-213A>G
XM_011514087.1:c.-170A>G (CPLANE1)	XP_011512389.1:n.-170A>G
XM_011514088.1:c.-170A>G (CPLANE1)	XP_011512390.1:n.-170A>G
XM_011514089.1:c.-170A>G (CPLANE1)	XP_011512391.1:n.-170A>G
XM_011514090.1:c.-407A>G (CPLANE1)	XP_011512392.1:n.-407A>G
XM_011514092.1:c.-170A>G (CPLANE1)	XP_011512394.1:n.-170A>G
XM_011514093.1:c.-170A>G (CPLANE1)	XP_011512395.1:n.-170A>G
XR_427661.2:n.6A>G (CPLANE1)
XR_925644.1:n.6A>G (CPLANE1)
XR_925921.1:n.171+146T>C (CPLANE1-AS1)
NR_134263.1:n.176+146T>C (CPLANE1-AS1)
XM_005248345.4:c.-170A>G (CPLANE1)	XP_005248402.1:n.-170A>G
XM_005248346.4:c.-170A>G (CPLANE1)	XP_005248403.1:n.-170A>G
XM_005248347.4:c.-170A>G (CPLANE1)	XP_005248404.1:n.-170A>G
XM_005248349.4:c.-170A>G (CPLANE1)	XP_005248406.1:n.-170A>G
XM_005248350.4:c.-170A>G (CPLANE1)	XP_005248407.1:n.-170A>G
XM_011514086.3:c.-213A>G (CPLANE1)	XP_011512388.1:n.-213A>G
XM_011514087.2:c.-170A>G (CPLANE1)	XP_011512389.1:n.-170A>G
XM_011514088.2:c.-170A>G (CPLANE1)	XP_011512390.1:n.-170A>G
XM_011514089.2:c.-170A>G (CPLANE1)	XP_011512391.1:n.-170A>G
XM_011514090.3:c.-407A>G (CPLANE1)	XP_011512392.1:n.-407A>G
XM_011514092.2:c.-170A>G (CPLANE1)	XP_011512394.1:n.-170A>G
XM_017009761.2:c.-142A>G (CPLANE1)	XP_016865250.1:n.-142A>G
XM_017009765.1:c.-1101A>G (CPLANE1)	XP_016865254.1:n.-1101A>G
XM_024446184.1:c.-450A>G (CPLANE1)	XP_024301952.1:n.-450A>G
XM_024446185.1:c.-697A>G (CPLANE1)	XP_024301953.1:n.-697A>G
XM_024446186.1:c.-1168A>G (CPLANE1)	XP_024301954.1:n.-1168A>G
XR_001742208.1:n.55A>G (CPLANE1)
XR_002956171.1:n.55A>G (CPLANE1)
XR_925644.2:n.55A>G (CPLANE1)
NM_001384732.1:c.-170A>G (CPLANE1) MANE Select	NP_001371661.1:n.-170A>G
NM_023073.4:c.-170A>G (CPLANE1)	NP_075561.3:n.-170A>G