Canonical Allele Identifier: CA1058852469

Gene: EVC CRMP1

Linked Data

• dbSNP Id: rs1716236669
• gnomAD v3: 4-5808130-T-TCTAC
• gnomAD v4: 4-5808130-T-TCTAC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5808132_5808133insACCT , CM000666.2:g.5808132_5808133insACCT	GRCh38
NC_000004.11:g.5809859_5809860insACCT , CM000666.1:g.5809859_5809860insACCT	GRCh37
NC_000004.10:g.5860760_5860761insACCT	NCBI36
NG_008843.1:g.101936_101937insACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.2562-69_2562-68insACCT (EVC) MANE Select	ENSP00000264956.6:n.2562-69_2562-68insACCT
ENST00000264956.10:c.2562-69_2562-68insACCT (EVC)	ENSP00000264956.6:n.2562-69_2562-68insACCT
ENST00000506216.5:n.1647+17363_1647+17364insGTAG (CRMP1)
NM_001306090.1:c.2562-69_2562-68insACCT (EVC)	NP_001293019.1:n.2562-69_2562-68insACCT
NM_153717.2:c.2562-69_2562-68insACCT (EVC)	NP_714928.1:n.2562-69_2562-68insACCT
XM_006713865.2:c.2562-69_2562-68insACCT (EVC)	XP_006713928.1:n.2562-69_2562-68insACCT
XM_006713866.2:c.2562-69_2562-68insACCT (EVC)	XP_006713929.1:n.2562-69_2562-68insACCT
XR_427473.2:n.2752-69_2752-68insACCT (EVC)
XR_427475.2:n.2752-69_2752-68insACCT (EVC)
XR_427476.2:n.2752-69_2752-68insACCT (EVC)
XR_924920.1:n.2752-69_2752-68insACCT (EVC)
XR_924921.1:n.2752-69_2752-68insACCT (EVC)
XR_924922.1:n.2752-69_2752-68insACCT (EVC)
XR_924923.1:n.2752-69_2752-68insACCT (EVC)
XR_924924.1:n.2752-69_2752-68insACCT (EVC)
XR_924925.1:n.2752-69_2752-68insACCT (EVC)
XR_924926.1:n.2752-69_2752-68insACCT (EVC)
XR_924927.1:n.2752-69_2752-68insACCT (EVC)
XM_006713865.3:c.2562-69_2562-68insACCT (EVC)	XP_006713928.1:n.2562-69_2562-68insACCT
XM_006713866.3:c.2562-69_2562-68insACCT (EVC)	XP_006713929.1:n.2562-69_2562-68insACCT
XR_001741164.1:n.2742-69_2742-68insACCT (EVC)
XR_001741165.1:n.2742-69_2742-68insACCT (EVC)
XR_001741166.1:n.2742-69_2742-68insACCT (EVC)
XR_001741167.1:n.2742-69_2742-68insACCT (EVC)
XR_001741168.1:n.2742-69_2742-68insACCT (EVC)
XR_001741169.2:n.2606-69_2606-68insACCT (EVC)
XR_001741170.1:n.2827-69_2827-68insACCT (EVC)
XR_001741171.1:n.2047-69_2047-68insACCT (EVC)
XR_427473.3:n.2742-69_2742-68insACCT (EVC)
XR_427475.3:n.2742-69_2742-68insACCT (EVC)
XR_427476.3:n.2742-69_2742-68insACCT (EVC)
XR_924920.2:n.2742-69_2742-68insACCT (EVC)
XR_924921.2:n.2742-69_2742-68insACCT (EVC)
XR_924922.2:n.2742-69_2742-68insACCT (EVC)
XR_924924.2:n.2742-69_2742-68insACCT (EVC)
XR_924925.2:n.2742-69_2742-68insACCT (EVC)
XR_924926.2:n.2742-69_2742-68insACCT (EVC)
NM_153717.3:c.2562-69_2562-68insACCT (EVC) MANE Select	NP_714928.1:n.2562-69_2562-68insACCT
NM_001306090.2:c.2562-69_2562-68insACCT (EVC)	NP_001293019.1:n.2562-69_2562-68insACCT