Canonical Allele Identifier: CA2669814207

Gene: EVC CRMP1

Linked Data

• gnomAD v4: 4-5808475-G-GCCGACACACCCTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5808475_5808476insCCGACACACCCTCA , CM000666.2:g.5808475_5808476insCCGACACACCCTCA	GRCh38
NC_000004.11:g.5810202_5810203insCCGACACACCCTCA , CM000666.1:g.5810202_5810203insCCGACACACCCTCA	GRCh37
NC_000004.10:g.5861103_5861104insCCGACACACCCTCA	NCBI36
NG_008843.1:g.102279_102280insCCGACACACCCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.2688+148_2688+149insCCGACACACCCTCA (EVC) MANE Select	ENSP00000264956.6:n.2688+148_2688+149insCCGACACACCCTCA
ENST00000264956.10:c.2688+148_2688+149insCCGACACACCCTCA (EVC)	ENSP00000264956.6:n.2688+148_2688+149insCCGACACACCCTCA
ENST00000506216.5:n.1647+17018_1647+17019insTGAGGGTGTGTCGG (CRMP1)
NM_001306090.1:c.2688+148_2688+149insCCGACACACCCTCA (EVC)	NP_001293019.1:n.2688+148_2688+149insCCGACACACCCTCA
NM_153717.2:c.2688+148_2688+149insCCGACACACCCTCA (EVC)	NP_714928.1:n.2688+148_2688+149insCCGACACACCCTCA
XM_006713865.2:c.2688+148_2688+149insCCGACACACCCTCA (EVC)	XP_006713928.1:n.2688+148_2688+149insCCGACACACCCTCA
XM_006713866.2:c.2688+148_2688+149insCCGACACACCCTCA (EVC)	XP_006713929.1:n.2688+148_2688+149insCCGACACACCCTCA
XR_427473.2:n.2878+148_2878+149insCCGACACACCCTCA (EVC)
XR_427475.2:n.2878+148_2878+149insCCGACACACCCTCA (EVC)
XR_427476.2:n.2878+148_2878+149insCCGACACACCCTCA (EVC)
XR_924920.1:n.2878+148_2878+149insCCGACACACCCTCA (EVC)
XR_924921.1:n.2878+148_2878+149insCCGACACACCCTCA (EVC)
XR_924922.1:n.2878+148_2878+149insCCGACACACCCTCA (EVC)
XR_924923.1:n.2878+148_2878+149insCCGACACACCCTCA (EVC)
XR_924924.1:n.2878+148_2878+149insCCGACACACCCTCA (EVC)
XR_924925.1:n.2878+148_2878+149insCCGACACACCCTCA (EVC)
XR_924926.1:n.2878+148_2878+149insCCGACACACCCTCA (EVC)
XR_924927.1:n.2878+148_2878+149insCCGACACACCCTCA (EVC)
XM_006713865.3:c.2688+148_2688+149insCCGACACACCCTCA (EVC)	XP_006713928.1:n.2688+148_2688+149insCCGACACACCCTCA
XM_006713866.3:c.2688+148_2688+149insCCGACACACCCTCA (EVC)	XP_006713929.1:n.2688+148_2688+149insCCGACACACCCTCA
XR_001741164.1:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_001741165.1:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_001741166.1:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_001741167.1:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_001741168.1:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_001741169.2:n.2732+148_2732+149insCCGACACACCCTCA (EVC)
XR_001741170.1:n.2953+148_2953+149insCCGACACACCCTCA (EVC)
XR_001741171.1:n.2173+148_2173+149insCCGACACACCCTCA (EVC)
XR_427473.3:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_427475.3:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_427476.3:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_924920.2:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_924921.2:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_924922.2:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_924924.2:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_924925.2:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
XR_924926.2:n.2868+148_2868+149insCCGACACACCCTCA (EVC)
NM_153717.3:c.2688+148_2688+149insCCGACACACCCTCA (EVC) MANE Select	NP_714928.1:n.2688+148_2688+149insCCGACACACCCTCA
NM_001306090.2:c.2688+148_2688+149insCCGACACACCCTCA (EVC)	NP_001293019.1:n.2688+148_2688+149insCCGACACACCCTCA