Canonical Allele Identifier: CA2765920489
Gene: CPLANE1 HGNC NCBI
CPLANE1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37249384G>A , CM000667.2:g.37249384G>A GRCh38
NC_000005.9:g.37249486G>A , CM000667.1:g.37249486G>A GRCh37
NC_000005.8:g.37285243G>A NCBI36
NG_032772.1:g.5045C>T
NG_032772.2:g.5045C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000425232.6:c.-187C>T (CPLANE1) ENSP00000389014.2:n.-187C>T
NM_023073.3:c.-187C>T (CPLANE1) NP_075561.3:n.-187C>T
XR_925921.1:n.171+163G>A (CPLANE1-AS1)
NR_134263.1:n.176+163G>A (CPLANE1-AS1)
XM_005248345.4:c.-187C>T (CPLANE1) XP_005248402.1:n.-187C>T
XM_005248346.4:c.-187C>T (CPLANE1) XP_005248403.1:n.-187C>T
XM_005248347.4:c.-187C>T (CPLANE1) XP_005248404.1:n.-187C>T
XM_005248349.4:c.-187C>T (CPLANE1) XP_005248406.1:n.-187C>T
XM_005248350.4:c.-187C>T (CPLANE1) XP_005248407.1:n.-187C>T
XM_011514086.3:c.-230C>T (CPLANE1) XP_011512388.1:n.-230C>T
XM_011514087.2:c.-187C>T (CPLANE1) XP_011512389.1:n.-187C>T
XM_011514088.2:c.-187C>T (CPLANE1) XP_011512390.1:n.-187C>T
XM_011514089.2:c.-187C>T (CPLANE1) XP_011512391.1:n.-187C>T
XM_011514090.3:c.-424C>T (CPLANE1) XP_011512392.1:n.-424C>T
XM_011514092.2:c.-187C>T (CPLANE1) XP_011512394.1:n.-187C>T
XM_017009761.2:c.-159C>T (CPLANE1) XP_016865250.1:n.-159C>T
XM_024446184.1:c.-467C>T (CPLANE1) XP_024301952.1:n.-467C>T
XM_024446185.1:c.-714C>T (CPLANE1) XP_024301953.1:n.-714C>T
XM_024446186.1:c.-1185C>T (CPLANE1) XP_024301954.1:n.-1185C>T
XR_001742208.1:n.38C>T (CPLANE1)
XR_002956171.1:n.38C>T (CPLANE1)
XR_925644.2:n.38C>T (CPLANE1)