Canonical Allele Identifier: CA1435493883

Gene: EVC CRMP1

Linked Data

• ClinVar Variation Id: 2937340
• ClinVar RCV Id: RCV003791530
• dbSNP Id: rs1731153761
• gnomAD v4: 4-5756248-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5756249_5756250dup , CM000666.2:g.5756249_5756250dup	GRCh38
NC_000004.11:g.5757976_5757977dup , CM000666.1:g.5757976_5757977dup	GRCh37
NC_000004.10:g.5808877_5808878dup	NCBI36
NG_008843.1:g.50053_50054dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.1465-15_1465-14dup (EVC) MANE Select	ENSP00000264956.6:n.1465-15_1465-14dup
ENST00000264956.10:c.1465-15_1465-14dup (EVC)	ENSP00000264956.6:n.1465-15_1465-14dup
ENST00000506216.5:n.1648-7938_1648-7937dup (CRMP1)
ENST00000509451.1:c.1465-15_1465-14dup (EVC)	ENSP00000426774.1:n.1465-15_1465-14dup
NM_001306090.1:c.1465-15_1465-14dup (EVC)	NP_001293019.1:n.1465-15_1465-14dup
NM_001306092.1:c.1465-15_1465-14dup (EVC)	NP_001293021.1:n.1465-15_1465-14dup
NM_153717.2:c.1465-15_1465-14dup (EVC)	NP_714928.1:n.1465-15_1465-14dup
XM_006713865.2:c.1465-15_1465-14dup (EVC)	XP_006713928.1:n.1465-15_1465-14dup
XM_006713866.2:c.1465-15_1465-14dup (EVC)	XP_006713929.1:n.1465-15_1465-14dup
XM_011513419.1:c.1465-15_1465-14dup (EVC)	XP_011511721.1:n.1465-15_1465-14dup
XR_427473.2:n.1655-15_1655-14dup (EVC)
XR_427475.2:n.1655-15_1655-14dup (EVC)
XR_427476.2:n.1655-15_1655-14dup (EVC)
XR_924920.1:n.1655-15_1655-14dup (EVC)
XR_924921.1:n.1655-15_1655-14dup (EVC)
XR_924922.1:n.1655-15_1655-14dup (EVC)
XR_924923.1:n.1655-15_1655-14dup (EVC)
XR_924924.1:n.1655-15_1655-14dup (EVC)
XR_924925.1:n.1655-15_1655-14dup (EVC)
XR_924926.1:n.1655-15_1655-14dup (EVC)
XR_924927.1:n.1655-15_1655-14dup (EVC)
XR_924928.1:n.1657-15_1657-14dup (EVC)
XM_006713865.3:c.1465-15_1465-14dup (EVC)	XP_006713928.1:n.1465-15_1465-14dup
XM_006713866.3:c.1465-15_1465-14dup (EVC)	XP_006713929.1:n.1465-15_1465-14dup
XM_011513419.2:c.1465-15_1465-14dup (EVC)	XP_011511721.1:n.1465-15_1465-14dup
XM_017007883.2:c.1465-15_1465-14dup (EVC)	XP_016863372.1:n.1465-15_1465-14dup
XR_001741164.1:n.1645-15_1645-14dup (EVC)
XR_001741165.1:n.1645-15_1645-14dup (EVC)
XR_001741166.1:n.1645-15_1645-14dup (EVC)
XR_001741167.1:n.1645-15_1645-14dup (EVC)
XR_001741168.1:n.1645-15_1645-14dup (EVC)
XR_001741169.2:n.1509-15_1509-14dup (EVC)
XR_001741170.1:n.1647-15_1647-14dup (EVC)
XR_001741171.1:n.950-15_950-14dup (EVC)
XR_427473.3:n.1645-15_1645-14dup (EVC)
XR_427475.3:n.1645-15_1645-14dup (EVC)
XR_427476.3:n.1645-15_1645-14dup (EVC)
XR_924920.2:n.1645-15_1645-14dup (EVC)
XR_924921.2:n.1645-15_1645-14dup (EVC)
XR_924922.2:n.1645-15_1645-14dup (EVC)
XR_924924.2:n.1645-15_1645-14dup (EVC)
XR_924925.2:n.1645-15_1645-14dup (EVC)
XR_924926.2:n.1645-15_1645-14dup (EVC)
NM_153717.3:c.1465-15_1465-14dup (EVC) MANE Select	NP_714928.1:n.1465-15_1465-14dup
NM_001306090.2:c.1465-15_1465-14dup (EVC)	NP_001293019.1:n.1465-15_1465-14dup
NM_001306092.2:c.1465-15_1465-14dup (EVC)	NP_001293021.1:n.1465-15_1465-14dup