Canonical Allele Identifier: CA359474316

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37154059C>G (hg19) ; chr5:g.37153957C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153957C>G , CM000667.2:g.37153957C>G	GRCh38
NC_000005.9:g.37154059C>G , CM000667.1:g.37154059C>G	GRCh37
NC_000005.8:g.37189816C>G	NCBI36
NG_032772.1:g.100472G>C
NG_032772.2:g.100472G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1155G>C
ENST00000651892.2:c.8156G>C MANE Select	ENSP00000498265.2:p.Ser2719Thr
ENST00000425232.6:c.7994G>C	ENSP00000389014.2:p.Ser2665Thr
ENST00000508244.5:c.7994G>C	ENSP00000421690.1:p.Ser2665Thr
ENST00000509849.5:c.5168G>C	ENSP00000426337.1:p.Ser1723Thr
ENST00000509957.5:n.398G>C
ENST00000511210.5:n.447G>C
ENST00000511824.2:c.1270G>C
ENST00000514429.5:c.5192G>C	ENSP00000424223.1:p.Ser1731Thr
ENST00000515380.1:n.408G>C
NM_023073.3:c.7994G>C	NP_075561.3:p.Ser2665Thr
XM_005248345.2:c.8156G>C	XP_005248402.1:p.Ser2719Thr
XM_005248346.2:c.8153G>C	XP_005248403.1:p.Ser2718Thr
XM_005248347.2:c.8153G>C	XP_005248404.1:p.Ser2718Thr
XM_005248349.2:c.8045G>C	XP_005248406.1:p.Ser2682Thr
XM_005248350.2:c.8027G>C	XP_005248407.1:p.Ser2676Thr
XM_005248353.3:c.4799G>C	XP_005248410.1:p.Ser1600Thr
XM_006714489.2:c.8156G>C	XP_006714552.1:p.Ser2719Thr
XM_006714491.2:c.2729G>C	XP_006714554.1:p.Ser910Thr
XM_011514085.1:c.8156G>C	XP_011512387.1:p.Ser2719Thr
XM_011514086.1:c.8156G>C	XP_011512388.1:p.Ser2719Thr
XM_011514087.1:c.8102G>C	XP_011512389.1:p.Ser2701Thr
XM_011514088.1:c.8048G>C	XP_011512390.1:p.Ser2683Thr
XM_011514089.1:c.8156G>C	XP_011512391.1:p.Ser2719Thr
XM_011514090.1:c.7838G>C	XP_011512392.1:p.Ser2613Thr
XM_011514091.1:c.7484G>C	XP_011512393.1:p.Ser2495Thr
XM_011514092.1:c.8156G>C	XP_011512394.1:p.Ser2719Thr
XM_011514094.1:c.5381G>C	XP_011512396.1:p.Ser1794Thr
XR_427661.2:n.8331G>C
XR_925644.1:n.8331G>C
XM_005248345.4:c.8156G>C	XP_005248402.1:p.Ser2719Thr
XM_005248346.4:c.8153G>C	XP_005248403.1:p.Ser2718Thr
XM_005248347.4:c.8153G>C	XP_005248404.1:p.Ser2718Thr
XM_005248349.4:c.8045G>C	XP_005248406.1:p.Ser2682Thr
XM_005248350.4:c.8027G>C	XP_005248407.1:p.Ser2676Thr
XM_006714491.3:c.2729G>C	XP_006714554.1:p.Ser910Thr
XM_011514085.3:c.8156G>C	XP_011512387.1:p.Ser2719Thr
XM_011514086.3:c.8156G>C	XP_011512388.1:p.Ser2719Thr
XM_011514087.2:c.8102G>C	XP_011512389.1:p.Ser2701Thr
XM_011514088.2:c.8048G>C	XP_011512390.1:p.Ser2683Thr
XM_011514089.2:c.8156G>C	XP_011512391.1:p.Ser2719Thr
XM_011514090.3:c.7838G>C	XP_011512392.1:p.Ser2613Thr
XM_011514092.2:c.8156G>C	XP_011512394.1:p.Ser2719Thr
XM_011514094.2:c.5381G>C	XP_011512396.1:p.Ser1794Thr
XM_017009760.1:c.7967G>C	XP_016865249.1:p.Ser2656Thr
XM_017009761.2:c.7967G>C	XP_016865250.1:p.Ser2656Thr
XM_017009763.1:c.7163G>C	XP_016865252.1:p.Ser2388Thr
XM_017009765.1:c.6968G>C	XP_016865254.1:p.Ser2323Thr
XM_017009766.1:c.4799G>C	XP_016865255.1:p.Ser1600Thr
XM_024446183.1:c.7967G>C	XP_024301951.1:p.Ser2656Thr
XM_024446184.1:c.7838G>C	XP_024301952.1:p.Ser2613Thr
XM_024446185.1:c.7484G>C	XP_024301953.1:p.Ser2495Thr
XM_024446186.1:c.7163G>C	XP_024301954.1:p.Ser2388Thr
XR_001742208.1:n.8325G>C
XR_002956171.1:n.8271G>C
XR_925644.2:n.8380G>C
NM_001384732.1:c.8156G>C MANE Select	NP_001371661.1:p.Ser2719Thr
NM_023073.4:c.7994G>C	NP_075561.3:p.Ser2665Thr