Canonical Allele Identifier: CA1435493863

Gene: EVC CRMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5756223_5756225delinsCTG , CM000666.2:g.5756223_5756225delinsCTG	GRCh38
NC_000004.11:g.5757950_5757952delinsCTG , CM000666.1:g.5757950_5757952delinsCTG	GRCh37
NC_000004.10:g.5808851_5808853delinsCTG	NCBI36
NG_008843.1:g.50027_50029delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.1465-41_1465-39delinsCTG (EVC) MANE Select	ENSP00000264956.6:n.1465-41_1465-39delinsCTG
ENST00000264956.10:c.1465-41_1465-39delinsCTG (EVC)	ENSP00000264956.6:n.1465-41_1465-39delinsCTG
ENST00000506216.5:n.1648-7913_1648-7911delinsCAG (CRMP1)
ENST00000509451.1:c.1465-41_1465-39delinsCTG (EVC)	ENSP00000426774.1:n.1465-41_1465-39delinsCTG
NM_001306090.1:c.1465-41_1465-39delinsCTG (EVC)	NP_001293019.1:n.1465-41_1465-39delinsCTG
NM_001306092.1:c.1465-41_1465-39delinsCTG (EVC)	NP_001293021.1:n.1465-41_1465-39delinsCTG
NM_153717.2:c.1465-41_1465-39delinsCTG (EVC)	NP_714928.1:n.1465-41_1465-39delinsCTG
XM_006713865.2:c.1465-41_1465-39delinsCTG (EVC)	XP_006713928.1:n.1465-41_1465-39delinsCTG
XM_006713866.2:c.1465-41_1465-39delinsCTG (EVC)	XP_006713929.1:n.1465-41_1465-39delinsCTG
XM_011513419.1:c.1465-41_1465-39delinsCTG (EVC)	XP_011511721.1:n.1465-41_1465-39delinsCTG
XR_427473.2:n.1655-41_1655-39delinsCTG (EVC)
XR_427475.2:n.1655-41_1655-39delinsCTG (EVC)
XR_427476.2:n.1655-41_1655-39delinsCTG (EVC)
XR_924920.1:n.1655-41_1655-39delinsCTG (EVC)
XR_924921.1:n.1655-41_1655-39delinsCTG (EVC)
XR_924922.1:n.1655-41_1655-39delinsCTG (EVC)
XR_924923.1:n.1655-41_1655-39delinsCTG (EVC)
XR_924924.1:n.1655-41_1655-39delinsCTG (EVC)
XR_924925.1:n.1655-41_1655-39delinsCTG (EVC)
XR_924926.1:n.1655-41_1655-39delinsCTG (EVC)
XR_924927.1:n.1655-41_1655-39delinsCTG (EVC)
XR_924928.1:n.1657-41_1657-39delinsCTG (EVC)
XM_006713865.3:c.1465-41_1465-39delinsCTG (EVC)	XP_006713928.1:n.1465-41_1465-39delinsCTG
XM_006713866.3:c.1465-41_1465-39delinsCTG (EVC)	XP_006713929.1:n.1465-41_1465-39delinsCTG
XM_011513419.2:c.1465-41_1465-39delinsCTG (EVC)	XP_011511721.1:n.1465-41_1465-39delinsCTG
XM_017007883.2:c.1465-41_1465-39delinsCTG (EVC)	XP_016863372.1:n.1465-41_1465-39delinsCTG
XR_001741164.1:n.1645-41_1645-39delinsCTG (EVC)
XR_001741165.1:n.1645-41_1645-39delinsCTG (EVC)
XR_001741166.1:n.1645-41_1645-39delinsCTG (EVC)
XR_001741167.1:n.1645-41_1645-39delinsCTG (EVC)
XR_001741168.1:n.1645-41_1645-39delinsCTG (EVC)
XR_001741169.2:n.1509-41_1509-39delinsCTG (EVC)
XR_001741170.1:n.1647-41_1647-39delinsCTG (EVC)
XR_001741171.1:n.950-41_950-39delinsCTG (EVC)
XR_427473.3:n.1645-41_1645-39delinsCTG (EVC)
XR_427475.3:n.1645-41_1645-39delinsCTG (EVC)
XR_427476.3:n.1645-41_1645-39delinsCTG (EVC)
XR_924920.2:n.1645-41_1645-39delinsCTG (EVC)
XR_924921.2:n.1645-41_1645-39delinsCTG (EVC)
XR_924922.2:n.1645-41_1645-39delinsCTG (EVC)
XR_924924.2:n.1645-41_1645-39delinsCTG (EVC)
XR_924925.2:n.1645-41_1645-39delinsCTG (EVC)
XR_924926.2:n.1645-41_1645-39delinsCTG (EVC)
NM_153717.3:c.1465-41_1465-39delinsCTG (EVC) MANE Select	NP_714928.1:n.1465-41_1465-39delinsCTG
NM_001306090.2:c.1465-41_1465-39delinsCTG (EVC)	NP_001293019.1:n.1465-41_1465-39delinsCTG
NM_001306092.2:c.1465-41_1465-39delinsCTG (EVC)	NP_001293021.1:n.1465-41_1465-39delinsCTG