Canonical Allele Identifier: CA1539711310
Gene: CPLANE1 HGNC NCBI
CPLANE1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1740985354
gnomAD v4: 5-37249352-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37249352T>C , CM000667.2:g.37249352T>C GRCh38
NC_000005.9:g.37249454T>C , CM000667.1:g.37249454T>C GRCh37
NC_000005.8:g.37285211T>C NCBI36
NG_032772.1:g.5077A>G
NG_032772.2:g.5077A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651892.2:c.-155A>G (CPLANE1) MANE Select ENSP00000498265.2:n.-155A>G
ENST00000675547.1:n.14A>G (CPLANE1)
ENST00000425232.6:c.-155A>G (CPLANE1) ENSP00000389014.2:n.-155A>G
NM_023073.3:c.-155A>G (CPLANE1) NP_075561.3:n.-155A>G
XM_005248345.2:c.-155A>G (CPLANE1) XP_005248402.1:n.-155A>G
XM_005248346.2:c.-155A>G (CPLANE1) XP_005248403.1:n.-155A>G
XM_005248347.2:c.-155A>G (CPLANE1) XP_005248404.1:n.-155A>G
XM_005248349.2:c.-155A>G (CPLANE1) XP_005248406.1:n.-155A>G
XM_005248350.2:c.-155A>G (CPLANE1) XP_005248407.1:n.-155A>G
XM_006714489.2:c.-155A>G (CPLANE1) XP_006714552.1:n.-155A>G
XM_011514086.1:c.-198A>G (CPLANE1) XP_011512388.1:n.-198A>G
XM_011514087.1:c.-155A>G (CPLANE1) XP_011512389.1:n.-155A>G
XM_011514088.1:c.-155A>G (CPLANE1) XP_011512390.1:n.-155A>G
XM_011514089.1:c.-155A>G (CPLANE1) XP_011512391.1:n.-155A>G
XM_011514090.1:c.-392A>G (CPLANE1) XP_011512392.1:n.-392A>G
XM_011514092.1:c.-155A>G (CPLANE1) XP_011512394.1:n.-155A>G
XM_011514093.1:c.-155A>G (CPLANE1) XP_011512395.1:n.-155A>G
XR_427661.2:n.21A>G (CPLANE1)
XR_925644.1:n.21A>G (CPLANE1)
XR_925921.1:n.171+131T>C (CPLANE1-AS1)
NR_134263.1:n.176+131T>C (CPLANE1-AS1)
XM_005248345.4:c.-155A>G (CPLANE1) XP_005248402.1:n.-155A>G
XM_005248346.4:c.-155A>G (CPLANE1) XP_005248403.1:n.-155A>G
XM_005248347.4:c.-155A>G (CPLANE1) XP_005248404.1:n.-155A>G
XM_005248349.4:c.-155A>G (CPLANE1) XP_005248406.1:n.-155A>G
XM_005248350.4:c.-155A>G (CPLANE1) XP_005248407.1:n.-155A>G
XM_011514086.3:c.-198A>G (CPLANE1) XP_011512388.1:n.-198A>G
XM_011514087.2:c.-155A>G (CPLANE1) XP_011512389.1:n.-155A>G
XM_011514088.2:c.-155A>G (CPLANE1) XP_011512390.1:n.-155A>G
XM_011514089.2:c.-155A>G (CPLANE1) XP_011512391.1:n.-155A>G
XM_011514090.3:c.-392A>G (CPLANE1) XP_011512392.1:n.-392A>G
XM_011514092.2:c.-155A>G (CPLANE1) XP_011512394.1:n.-155A>G
XM_017009761.2:c.-127A>G (CPLANE1) XP_016865250.1:n.-127A>G
XM_017009765.1:c.-1086A>G (CPLANE1) XP_016865254.1:n.-1086A>G
XM_024446184.1:c.-435A>G (CPLANE1) XP_024301952.1:n.-435A>G
XM_024446185.1:c.-682A>G (CPLANE1) XP_024301953.1:n.-682A>G
XM_024446186.1:c.-1153A>G (CPLANE1) XP_024301954.1:n.-1153A>G
XR_001742208.1:n.70A>G (CPLANE1)
XR_002956171.1:n.70A>G (CPLANE1)
XR_925644.2:n.70A>G (CPLANE1)
NM_001384732.1:c.-155A>G (CPLANE1) MANE Select NP_001371661.1:n.-155A>G
NM_023073.4:c.-155A>G (CPLANE1) NP_075561.3:n.-155A>G