Canonical Allele Identifier: CA1435523053

Gene: EVC CRMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5808609_5808611delinsCAG , CM000666.2:g.5808609_5808611delinsCAG	GRCh38
NC_000004.11:g.5810336_5810338delinsCAG , CM000666.1:g.5810336_5810338delinsCAG	GRCh37
NC_000004.10:g.5861237_5861239delinsCAG	NCBI36
NG_008843.1:g.102413_102415delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.2688+282_2688+284delinsCAG (EVC) MANE Select	ENSP00000264956.6:n.2688+282_2688+284delinsCAG
ENST00000264956.10:c.2688+282_2688+284delinsCAG (EVC)	ENSP00000264956.6:n.2688+282_2688+284delinsCAG
ENST00000506216.5:n.1647+16883_1647+16885delinsCTG (CRMP1)
NM_001306090.1:c.2688+282_2688+284delinsCAG (EVC)	NP_001293019.1:n.2688+282_2688+284delinsCAG
NM_153717.2:c.2688+282_2688+284delinsCAG (EVC)	NP_714928.1:n.2688+282_2688+284delinsCAG
XM_006713865.2:c.2688+282_2688+284delinsCAG (EVC)	XP_006713928.1:n.2688+282_2688+284delinsCAG
XM_006713866.2:c.2688+282_2688+284delinsCAG (EVC)	XP_006713929.1:n.2688+282_2688+284delinsCAG
XR_427473.2:n.2878+282_2878+284delinsCAG (EVC)
XR_427475.2:n.2878+282_2878+284delinsCAG (EVC)
XR_427476.2:n.2878+282_2878+284delinsCAG (EVC)
XR_924920.1:n.2878+282_2878+284delinsCAG (EVC)
XR_924921.1:n.2878+282_2878+284delinsCAG (EVC)
XR_924922.1:n.2878+282_2878+284delinsCAG (EVC)
XR_924923.1:n.2878+282_2878+284delinsCAG (EVC)
XR_924924.1:n.2878+282_2878+284delinsCAG (EVC)
XR_924925.1:n.2878+282_2878+284delinsCAG (EVC)
XR_924926.1:n.2878+282_2878+284delinsCAG (EVC)
XR_924927.1:n.2878+282_2878+284delinsCAG (EVC)
XM_006713865.3:c.2688+282_2688+284delinsCAG (EVC)	XP_006713928.1:n.2688+282_2688+284delinsCAG
XM_006713866.3:c.2688+282_2688+284delinsCAG (EVC)	XP_006713929.1:n.2688+282_2688+284delinsCAG
XR_001741164.1:n.2868+282_2868+284delinsCAG (EVC)
XR_001741165.1:n.2868+282_2868+284delinsCAG (EVC)
XR_001741166.1:n.2868+282_2868+284delinsCAG (EVC)
XR_001741167.1:n.2868+282_2868+284delinsCAG (EVC)
XR_001741168.1:n.2868+282_2868+284delinsCAG (EVC)
XR_001741169.2:n.2732+282_2732+284delinsCAG (EVC)
XR_001741170.1:n.2953+282_2953+284delinsCAG (EVC)
XR_001741171.1:n.2173+282_2173+284delinsCAG (EVC)
XR_427473.3:n.2868+282_2868+284delinsCAG (EVC)
XR_427475.3:n.2868+282_2868+284delinsCAG (EVC)
XR_427476.3:n.2868+282_2868+284delinsCAG (EVC)
XR_924920.2:n.2868+282_2868+284delinsCAG (EVC)
XR_924921.2:n.2868+282_2868+284delinsCAG (EVC)
XR_924922.2:n.2868+282_2868+284delinsCAG (EVC)
XR_924924.2:n.2868+282_2868+284delinsCAG (EVC)
XR_924925.2:n.2868+282_2868+284delinsCAG (EVC)
XR_924926.2:n.2868+282_2868+284delinsCAG (EVC)
NM_153717.3:c.2688+282_2688+284delinsCAG (EVC) MANE Select	NP_714928.1:n.2688+282_2688+284delinsCAG
NM_001306090.2:c.2688+282_2688+284delinsCAG (EVC)	NP_001293019.1:n.2688+282_2688+284delinsCAG