Canonical Allele Identifier: CA359498688

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37125384C>A (hg19) ; chr5:g.37125282C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37125282C>A , CM000667.2:g.37125282C>A	GRCh38
NC_000005.9:g.37125384C>A , CM000667.1:g.37125384C>A	GRCh37
NC_000005.8:g.37161141C>A	NCBI36
NG_032772.1:g.129147G>T
NG_032772.2:g.129147G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1919G>T
ENST00000651892.2:c.8920G>T MANE Select	ENSP00000498265.2:p.Gly2974Trp
ENST00000676160.1:n.781G>T
ENST00000425232.6:c.8758G>T	ENSP00000389014.2:p.Gly2920Trp
ENST00000508244.5:c.8758G>T	ENSP00000421690.1:p.Gly2920Trp
ENST00000509849.5:c.5932G>T	ENSP00000426337.1:n.5932G>T
ENST00000509957.5:n.4101G>T
ENST00000512288.5:n.342-3498G>T
ENST00000514429.5:c.5956G>T	ENSP00000424223.1:p.Gly1986Trp
NM_023073.3:c.8758G>T	NP_075561.3:p.Gly2920Trp
XM_005248345.2:c.8920G>T	XP_005248402.1:p.Gly2974Trp
XM_005248346.2:c.8917G>T	XP_005248403.1:p.Gly2973Trp
XM_005248347.2:c.8917G>T	XP_005248404.1:p.Gly2973Trp
XM_005248349.2:c.8809G>T	XP_005248406.1:p.Gly2937Trp
XM_005248350.2:c.8791G>T	XP_005248407.1:p.Gly2931Trp
XM_005248353.3:c.5563G>T	XP_005248410.1:p.Gly1855Trp
XM_006714489.2:c.8920G>T	XP_006714552.1:p.Gly2974Trp
XM_006714491.2:c.3493G>T	XP_006714554.1:p.Gly1165Trp
XM_011514085.1:c.8920G>T	XP_011512387.1:p.Gly2974Trp
XM_011514086.1:c.8920G>T	XP_011512388.1:p.Gly2974Trp
XM_011514087.1:c.8866G>T	XP_011512389.1:p.Gly2956Trp
XM_011514088.1:c.8812G>T	XP_011512390.1:p.Gly2938Trp
XM_011514089.1:c.8920G>T	XP_011512391.1:p.Gly2974Trp
XM_011514090.1:c.8602G>T	XP_011512392.1:p.Gly2868Trp
XM_011514091.1:c.8248G>T	XP_011512393.1:p.Gly2750Trp
XM_011514092.1:c.8920G>T	XP_011512394.1:p.Gly2974Trp
XM_011514094.1:c.6145G>T	XP_011512396.1:p.Gly2049Trp
XR_427661.2:n.9095G>T
XR_925644.1:n.9095G>T
XM_005248345.4:c.8920G>T	XP_005248402.1:p.Gly2974Trp
XM_005248346.4:c.8917G>T	XP_005248403.1:p.Gly2973Trp
XM_005248347.4:c.8917G>T	XP_005248404.1:p.Gly2973Trp
XM_005248349.4:c.8809G>T	XP_005248406.1:p.Gly2937Trp
XM_005248350.4:c.8791G>T	XP_005248407.1:p.Gly2931Trp
XM_006714491.3:c.3493G>T	XP_006714554.1:p.Gly1165Trp
XM_011514085.3:c.8920G>T	XP_011512387.1:p.Gly2974Trp
XM_011514086.3:c.8920G>T	XP_011512388.1:p.Gly2974Trp
XM_011514087.2:c.8866G>T	XP_011512389.1:p.Gly2956Trp
XM_011514088.2:c.8812G>T	XP_011512390.1:p.Gly2938Trp
XM_011514089.2:c.8920G>T	XP_011512391.1:p.Gly2974Trp
XM_011514090.3:c.8602G>T	XP_011512392.1:p.Gly2868Trp
XM_011514092.2:c.8920G>T	XP_011512394.1:p.Gly2974Trp
XM_011514094.2:c.6145G>T	XP_011512396.1:p.Gly2049Trp
XM_017009760.1:c.8731G>T	XP_016865249.1:p.Gly2911Trp
XM_017009761.2:c.8731G>T	XP_016865250.1:p.Gly2911Trp
XM_017009763.1:c.7927G>T	XP_016865252.1:p.Gly2643Trp
XM_017009765.1:c.7732G>T	XP_016865254.1:p.Gly2578Trp
XM_017009766.1:c.5563G>T	XP_016865255.1:p.Gly1855Trp
XM_024446183.1:c.8731G>T	XP_024301951.1:p.Gly2911Trp
XM_024446184.1:c.8602G>T	XP_024301952.1:p.Gly2868Trp
XM_024446185.1:c.8248G>T	XP_024301953.1:p.Gly2750Trp
XM_024446186.1:c.7927G>T	XP_024301954.1:p.Gly2643Trp
XR_925644.2:n.9144G>T
NM_001384732.1:c.8920G>T MANE Select	NP_001371661.1:p.Gly2974Trp
NM_023073.4:c.8758G>T	NP_075561.3:p.Gly2920Trp