Canonical Allele Identifier: CA810319291

Gene: CPLANE1 CPLANE1-AS1

Linked Data

• dbSNP Id: rs1413355917
• gnomAD v3: 5-37249347-A-G
• gnomAD v4: 5-37249347-A-G
• MyVariant Identifiers: chr5:g.37249449A>G (hg19) ; chr5:g.37249347A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37249347A>G , CM000667.2:g.37249347A>G	GRCh38
NC_000005.9:g.37249449A>G , CM000667.1:g.37249449A>G	GRCh37
NC_000005.8:g.37285206A>G	NCBI36
NG_032772.1:g.5082T>C
NG_032772.2:g.5082T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000651892.2:c.-150T>C (CPLANE1) MANE Select	ENSP00000498265.2:n.-150T>C
ENST00000675547.1:n.19T>C (CPLANE1)
ENST00000425232.6:c.-150T>C (CPLANE1)	ENSP00000389014.2:n.-150T>C
NM_023073.3:c.-150T>C (CPLANE1)	NP_075561.3:n.-150T>C
XM_005248345.2:c.-150T>C (CPLANE1)	XP_005248402.1:n.-150T>C
XM_005248346.2:c.-150T>C (CPLANE1)	XP_005248403.1:n.-150T>C
XM_005248347.2:c.-150T>C (CPLANE1)	XP_005248404.1:n.-150T>C
XM_005248349.2:c.-150T>C (CPLANE1)	XP_005248406.1:n.-150T>C
XM_005248350.2:c.-150T>C (CPLANE1)	XP_005248407.1:n.-150T>C
XM_006714489.2:c.-150T>C (CPLANE1)	XP_006714552.1:n.-150T>C
XM_011514086.1:c.-193T>C (CPLANE1)	XP_011512388.1:n.-193T>C
XM_011514087.1:c.-150T>C (CPLANE1)	XP_011512389.1:n.-150T>C
XM_011514088.1:c.-150T>C (CPLANE1)	XP_011512390.1:n.-150T>C
XM_011514089.1:c.-150T>C (CPLANE1)	XP_011512391.1:n.-150T>C
XM_011514090.1:c.-387T>C (CPLANE1)	XP_011512392.1:n.-387T>C
XM_011514092.1:c.-150T>C (CPLANE1)	XP_011512394.1:n.-150T>C
XM_011514093.1:c.-150T>C (CPLANE1)	XP_011512395.1:n.-150T>C
XR_427661.2:n.26T>C (CPLANE1)
XR_925644.1:n.26T>C (CPLANE1)
XR_925921.1:n.171+126A>G (CPLANE1-AS1)
NR_134263.1:n.176+126A>G (CPLANE1-AS1)
XM_005248345.4:c.-150T>C (CPLANE1)	XP_005248402.1:n.-150T>C
XM_005248346.4:c.-150T>C (CPLANE1)	XP_005248403.1:n.-150T>C
XM_005248347.4:c.-150T>C (CPLANE1)	XP_005248404.1:n.-150T>C
XM_005248349.4:c.-150T>C (CPLANE1)	XP_005248406.1:n.-150T>C
XM_005248350.4:c.-150T>C (CPLANE1)	XP_005248407.1:n.-150T>C
XM_011514086.3:c.-193T>C (CPLANE1)	XP_011512388.1:n.-193T>C
XM_011514087.2:c.-150T>C (CPLANE1)	XP_011512389.1:n.-150T>C
XM_011514088.2:c.-150T>C (CPLANE1)	XP_011512390.1:n.-150T>C
XM_011514089.2:c.-150T>C (CPLANE1)	XP_011512391.1:n.-150T>C
XM_011514090.3:c.-387T>C (CPLANE1)	XP_011512392.1:n.-387T>C
XM_011514092.2:c.-150T>C (CPLANE1)	XP_011512394.1:n.-150T>C
XM_017009761.2:c.-122T>C (CPLANE1)	XP_016865250.1:n.-122T>C
XM_017009765.1:c.-1081T>C (CPLANE1)	XP_016865254.1:n.-1081T>C
XM_024446184.1:c.-430T>C (CPLANE1)	XP_024301952.1:n.-430T>C
XM_024446185.1:c.-677T>C (CPLANE1)	XP_024301953.1:n.-677T>C
XM_024446186.1:c.-1148T>C (CPLANE1)	XP_024301954.1:n.-1148T>C
XR_001742208.1:n.75T>C (CPLANE1)
XR_002956171.1:n.75T>C (CPLANE1)
XR_925644.2:n.75T>C (CPLANE1)
NM_001384732.1:c.-150T>C (CPLANE1) MANE Select	NP_001371661.1:n.-150T>C
NM_023073.4:c.-150T>C (CPLANE1)	NP_075561.3:n.-150T>C