Canonical Allele Identifier: CA559031357

Gene: CPLANE1 CPLANE1-AS1

Linked Data

• dbSNP Id: rs1405367036
• gnomAD v2: 5-37249482-G-T
• gnomAD v3: 5-37249380-G-T
• gnomAD v4: 5-37249380-G-T
• MyVariant Identifiers: chr5:g.37249482G>T (hg19) ; chr5:g.37249380G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37249380G>T , CM000667.2:g.37249380G>T	GRCh38
NC_000005.9:g.37249482G>T , CM000667.1:g.37249482G>T	GRCh37
NC_000005.8:g.37285239G>T	NCBI36
NG_032772.1:g.5049C>A
NG_032772.2:g.5049C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425232.6:c.-183C>A (CPLANE1)	ENSP00000389014.2:n.-183C>A
NM_023073.3:c.-183C>A (CPLANE1)	NP_075561.3:n.-183C>A
XR_925921.1:n.171+159G>T (CPLANE1-AS1)
NR_134263.1:n.176+159G>T (CPLANE1-AS1)
XM_005248345.4:c.-183C>A (CPLANE1)	XP_005248402.1:n.-183C>A
XM_005248346.4:c.-183C>A (CPLANE1)	XP_005248403.1:n.-183C>A
XM_005248347.4:c.-183C>A (CPLANE1)	XP_005248404.1:n.-183C>A
XM_005248349.4:c.-183C>A (CPLANE1)	XP_005248406.1:n.-183C>A
XM_005248350.4:c.-183C>A (CPLANE1)	XP_005248407.1:n.-183C>A
XM_011514086.3:c.-226C>A (CPLANE1)	XP_011512388.1:n.-226C>A
XM_011514087.2:c.-183C>A (CPLANE1)	XP_011512389.1:n.-183C>A
XM_011514088.2:c.-183C>A (CPLANE1)	XP_011512390.1:n.-183C>A
XM_011514089.2:c.-183C>A (CPLANE1)	XP_011512391.1:n.-183C>A
XM_011514090.3:c.-420C>A (CPLANE1)	XP_011512392.1:n.-420C>A
XM_011514092.2:c.-183C>A (CPLANE1)	XP_011512394.1:n.-183C>A
XM_017009761.2:c.-155C>A (CPLANE1)	XP_016865250.1:n.-155C>A
XM_024446184.1:c.-463C>A (CPLANE1)	XP_024301952.1:n.-463C>A
XM_024446185.1:c.-710C>A (CPLANE1)	XP_024301953.1:n.-710C>A
XM_024446186.1:c.-1181C>A (CPLANE1)	XP_024301954.1:n.-1181C>A
XR_001742208.1:n.42C>A (CPLANE1)
XR_002956171.1:n.42C>A (CPLANE1)
XR_925644.2:n.42C>A (CPLANE1)