Canonical Allele Identifier: CA2673591134

Gene: CPLANE1 CPLANE1-AS1

Linked Data

• gnomAD v4: 5-37249264-CGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37249265_37249266del , CM000667.2:g.37249265_37249266del	GRCh38
NC_000005.9:g.37249367_37249368del , CM000667.1:g.37249367_37249368del	GRCh37
NC_000005.8:g.37285124_37285125del	NCBI36
NG_032772.1:g.5163_5164del
NG_032772.2:g.5163_5164del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651892.2:c.-69_-68del (CPLANE1) MANE Select	ENSP00000498265.2:n.-69_-68del
ENST00000675547.1:n.100_101del (CPLANE1)
ENST00000425232.6:c.-69_-68del (CPLANE1)	ENSP00000389014.2:n.-69_-68del
NM_023073.3:c.-69_-68del (CPLANE1)	NP_075561.3:n.-69_-68del
XM_005248345.2:c.-69_-68del (CPLANE1)	XP_005248402.1:n.-69_-68del
XM_005248346.2:c.-69_-68del (CPLANE1)	XP_005248403.1:n.-69_-68del
XM_005248347.2:c.-69_-68del (CPLANE1)	XP_005248404.1:n.-69_-68del
XM_005248349.2:c.-69_-68del (CPLANE1)	XP_005248406.1:n.-69_-68del
XM_005248350.2:c.-69_-68del (CPLANE1)	XP_005248407.1:n.-69_-68del
XM_006714489.2:c.-69_-68del (CPLANE1)	XP_006714552.1:n.-69_-68del
XM_011514086.1:c.-112_-111del (CPLANE1)	XP_011512388.1:n.-112_-111del
XM_011514087.1:c.-69_-68del (CPLANE1)	XP_011512389.1:n.-69_-68del
XM_011514088.1:c.-69_-68del (CPLANE1)	XP_011512390.1:n.-69_-68del
XM_011514089.1:c.-69_-68del (CPLANE1)	XP_011512391.1:n.-69_-68del
XM_011514090.1:c.-306_-305del (CPLANE1)	XP_011512392.1:n.-306_-305del
XM_011514092.1:c.-69_-68del (CPLANE1)	XP_011512394.1:n.-69_-68del
XM_011514093.1:c.-69_-68del (CPLANE1)	XP_011512395.1:n.-69_-68del
XR_427661.2:n.107_108del (CPLANE1)
XR_925644.1:n.107_108del (CPLANE1)
XR_925921.1:n.171+44_171+45del (CPLANE1-AS1)
NR_134263.1:n.176+44_176+45del (CPLANE1-AS1)
XM_005248345.4:c.-69_-68del (CPLANE1)	XP_005248402.1:n.-69_-68del
XM_005248346.4:c.-69_-68del (CPLANE1)	XP_005248403.1:n.-69_-68del
XM_005248347.4:c.-69_-68del (CPLANE1)	XP_005248404.1:n.-69_-68del
XM_005248349.4:c.-69_-68del (CPLANE1)	XP_005248406.1:n.-69_-68del
XM_005248350.4:c.-69_-68del (CPLANE1)	XP_005248407.1:n.-69_-68del
XM_011514086.3:c.-112_-111del (CPLANE1)	XP_011512388.1:n.-112_-111del
XM_011514087.2:c.-69_-68del (CPLANE1)	XP_011512389.1:n.-69_-68del
XM_011514088.2:c.-69_-68del (CPLANE1)	XP_011512390.1:n.-69_-68del
XM_011514089.2:c.-69_-68del (CPLANE1)	XP_011512391.1:n.-69_-68del
XM_011514090.3:c.-306_-305del (CPLANE1)	XP_011512392.1:n.-306_-305del
XM_011514092.2:c.-69_-68del (CPLANE1)	XP_011512394.1:n.-69_-68del
XM_017009761.2:c.-41_-40del (CPLANE1)	XP_016865250.1:n.-41_-40del
XM_017009765.1:c.-1000_-999del (CPLANE1)	XP_016865254.1:n.-1000_-999del
XM_024446184.1:c.-349_-348del (CPLANE1)	XP_024301952.1:n.-349_-348del
XM_024446185.1:c.-596_-595del (CPLANE1)	XP_024301953.1:n.-596_-595del
XM_024446186.1:c.-1067_-1066del (CPLANE1)	XP_024301954.1:n.-1067_-1066del
XR_001742208.1:n.156_157del (CPLANE1)
XR_002956171.1:n.156_157del (CPLANE1)
XR_925644.2:n.156_157del (CPLANE1)
NM_001384732.1:c.-69_-68del (CPLANE1) MANE Select	NP_001371661.1:n.-69_-68del
NM_023073.4:c.-69_-68del (CPLANE1)	NP_075561.3:n.-69_-68del