Canonical Allele Identifier: CA359498907

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37125405T>A (hg19) ; chr5:g.37125303T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37125303T>A , CM000667.2:g.37125303T>A	GRCh38
NC_000005.9:g.37125405T>A , CM000667.1:g.37125405T>A	GRCh37
NC_000005.8:g.37161162T>A	NCBI36
NG_032772.1:g.129126A>T
NG_032772.2:g.129126A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1898A>T
ENST00000651892.2:c.8899A>T MANE Select	ENSP00000498265.2:p.Asn2967Tyr
ENST00000676160.1:n.760A>T
ENST00000425232.6:c.8737A>T	ENSP00000389014.2:p.Asn2913Tyr
ENST00000508244.5:c.8737A>T	ENSP00000421690.1:p.Asn2913Tyr
ENST00000509849.5:c.5911A>T	ENSP00000426337.1:n.5911A>T
ENST00000509957.5:n.4080A>T
ENST00000512288.5:n.342-3519A>T
ENST00000514429.5:c.5935A>T	ENSP00000424223.1:p.Asn1979Tyr
NM_023073.3:c.8737A>T	NP_075561.3:p.Asn2913Tyr
XM_005248345.2:c.8899A>T	XP_005248402.1:p.Asn2967Tyr
XM_005248346.2:c.8896A>T	XP_005248403.1:p.Asn2966Tyr
XM_005248347.2:c.8896A>T	XP_005248404.1:p.Asn2966Tyr
XM_005248349.2:c.8788A>T	XP_005248406.1:p.Asn2930Tyr
XM_005248350.2:c.8770A>T	XP_005248407.1:p.Asn2924Tyr
XM_005248353.3:c.5542A>T	XP_005248410.1:p.Asn1848Tyr
XM_006714489.2:c.8899A>T	XP_006714552.1:p.Asn2967Tyr
XM_006714491.2:c.3472A>T	XP_006714554.1:p.Asn1158Tyr
XM_011514085.1:c.8899A>T	XP_011512387.1:p.Asn2967Tyr
XM_011514086.1:c.8899A>T	XP_011512388.1:p.Asn2967Tyr
XM_011514087.1:c.8845A>T	XP_011512389.1:p.Asn2949Tyr
XM_011514088.1:c.8791A>T	XP_011512390.1:p.Asn2931Tyr
XM_011514089.1:c.8899A>T	XP_011512391.1:p.Asn2967Tyr
XM_011514090.1:c.8581A>T	XP_011512392.1:p.Asn2861Tyr
XM_011514091.1:c.8227A>T	XP_011512393.1:p.Asn2743Tyr
XM_011514092.1:c.8899A>T	XP_011512394.1:p.Asn2967Tyr
XM_011514094.1:c.6124A>T	XP_011512396.1:p.Asn2042Tyr
XR_427661.2:n.9074A>T
XR_925644.1:n.9074A>T
XM_005248345.4:c.8899A>T	XP_005248402.1:p.Asn2967Tyr
XM_005248346.4:c.8896A>T	XP_005248403.1:p.Asn2966Tyr
XM_005248347.4:c.8896A>T	XP_005248404.1:p.Asn2966Tyr
XM_005248349.4:c.8788A>T	XP_005248406.1:p.Asn2930Tyr
XM_005248350.4:c.8770A>T	XP_005248407.1:p.Asn2924Tyr
XM_006714491.3:c.3472A>T	XP_006714554.1:p.Asn1158Tyr
XM_011514085.3:c.8899A>T	XP_011512387.1:p.Asn2967Tyr
XM_011514086.3:c.8899A>T	XP_011512388.1:p.Asn2967Tyr
XM_011514087.2:c.8845A>T	XP_011512389.1:p.Asn2949Tyr
XM_011514088.2:c.8791A>T	XP_011512390.1:p.Asn2931Tyr
XM_011514089.2:c.8899A>T	XP_011512391.1:p.Asn2967Tyr
XM_011514090.3:c.8581A>T	XP_011512392.1:p.Asn2861Tyr
XM_011514092.2:c.8899A>T	XP_011512394.1:p.Asn2967Tyr
XM_011514094.2:c.6124A>T	XP_011512396.1:p.Asn2042Tyr
XM_017009760.1:c.8710A>T	XP_016865249.1:p.Asn2904Tyr
XM_017009761.2:c.8710A>T	XP_016865250.1:p.Asn2904Tyr
XM_017009763.1:c.7906A>T	XP_016865252.1:p.Asn2636Tyr
XM_017009765.1:c.7711A>T	XP_016865254.1:p.Asn2571Tyr
XM_017009766.1:c.5542A>T	XP_016865255.1:p.Asn1848Tyr
XM_024446183.1:c.8710A>T	XP_024301951.1:p.Asn2904Tyr
XM_024446184.1:c.8581A>T	XP_024301952.1:p.Asn2861Tyr
XM_024446185.1:c.8227A>T	XP_024301953.1:p.Asn2743Tyr
XM_024446186.1:c.7906A>T	XP_024301954.1:p.Asn2636Tyr
XR_925644.2:n.9123A>T
NM_001384732.1:c.8899A>T MANE Select	NP_001371661.1:p.Asn2967Tyr
NM_023073.4:c.8737A>T	NP_075561.3:p.Asn2913Tyr