Canonical Allele Identifier: CA2760269635

Gene: EVC CRMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5808500_5808501insGACTAACCCAGGGCGGA , CM000666.2:g.5808500_5808501insGACTAACCCAGGGCGGA	GRCh38
NC_000004.11:g.5810227_5810228insGACTAACCCAGGGCGGA , CM000666.1:g.5810227_5810228insGACTAACCCAGGGCGGA	GRCh37
NC_000004.10:g.5861128_5861129insGACTAACCCAGGGCGGA	NCBI36
NG_008843.1:g.102304_102305insGACTAACCCAGGGCGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.2688+173_2688+174insGACTAACCCAGGGCGGA (EVC) MANE Select	ENSP00000264956.6:n.2688+173_2688+174insGACTAACCCAGGGCGGA
ENST00000264956.10:c.2688+173_2688+174insGACTAACCCAGGGCGGA (EVC)	ENSP00000264956.6:n.2688+173_2688+174insGACTAACCCAGGGCGGA
ENST00000506216.5:n.1647+16993_1647+16994insTCCGCCCTGGGTTAGTC (CRMP1)
NM_001306090.1:c.2688+173_2688+174insGACTAACCCAGGGCGGA (EVC)	NP_001293019.1:n.2688+173_2688+174insGACTAACCCAGGGCGGA
NM_153717.2:c.2688+173_2688+174insGACTAACCCAGGGCGGA (EVC)	NP_714928.1:n.2688+173_2688+174insGACTAACCCAGGGCGGA
XM_006713865.2:c.2688+173_2688+174insGACTAACCCAGGGCGGA (EVC)	XP_006713928.1:n.2688+173_2688+174insGACTAACCCAGGGCGGA
XM_006713866.2:c.2688+173_2688+174insGACTAACCCAGGGCGGA (EVC)	XP_006713929.1:n.2688+173_2688+174insGACTAACCCAGGGCGGA
XR_427473.2:n.2878+173_2878+174insGACTAACCCAGGGCGGA (EVC)
XR_427475.2:n.2878+173_2878+174insGACTAACCCAGGGCGGA (EVC)
XR_427476.2:n.2878+173_2878+174insGACTAACCCAGGGCGGA (EVC)
XR_924920.1:n.2878+173_2878+174insGACTAACCCAGGGCGGA (EVC)
XR_924921.1:n.2878+173_2878+174insGACTAACCCAGGGCGGA (EVC)
XR_924922.1:n.2878+173_2878+174insGACTAACCCAGGGCGGA (EVC)
XR_924923.1:n.2878+173_2878+174insGACTAACCCAGGGCGGA (EVC)
XR_924924.1:n.2878+173_2878+174insGACTAACCCAGGGCGGA (EVC)
XR_924925.1:n.2878+173_2878+174insGACTAACCCAGGGCGGA (EVC)
XR_924926.1:n.2878+173_2878+174insGACTAACCCAGGGCGGA (EVC)
XR_924927.1:n.2878+173_2878+174insGACTAACCCAGGGCGGA (EVC)
XM_006713865.3:c.2688+173_2688+174insGACTAACCCAGGGCGGA (EVC)	XP_006713928.1:n.2688+173_2688+174insGACTAACCCAGGGCGGA
XM_006713866.3:c.2688+173_2688+174insGACTAACCCAGGGCGGA (EVC)	XP_006713929.1:n.2688+173_2688+174insGACTAACCCAGGGCGGA
XR_001741164.1:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_001741165.1:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_001741166.1:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_001741167.1:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_001741168.1:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_001741169.2:n.2732+173_2732+174insGACTAACCCAGGGCGGA (EVC)
XR_001741170.1:n.2953+173_2953+174insGACTAACCCAGGGCGGA (EVC)
XR_001741171.1:n.2173+173_2173+174insGACTAACCCAGGGCGGA (EVC)
XR_427473.3:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_427475.3:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_427476.3:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_924920.2:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_924921.2:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_924922.2:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_924924.2:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_924925.2:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
XR_924926.2:n.2868+173_2868+174insGACTAACCCAGGGCGGA (EVC)
NM_153717.3:c.2688+173_2688+174insGACTAACCCAGGGCGGA (EVC) MANE Select	NP_714928.1:n.2688+173_2688+174insGACTAACCCAGGGCGGA
NM_001306090.2:c.2688+173_2688+174insGACTAACCCAGGGCGGA (EVC)	NP_001293019.1:n.2688+173_2688+174insGACTAACCCAGGGCGGA