Canonical Allele Identifier: CA549408250

Gene: EVC CRMP1

Linked Data

• gnomAD v2: 4-5809904-G-GTCCCTCCCTCCCTCTCTC
• gnomAD v3: 4-5808177-G-GTCCCTCCCTCCCTCTCTC
• gnomAD v4: 4-5808177-G-GTCCCTCCCTCCCTCTCTC
• MyVariant Identifiers: chr4:g.5809904_5809905insTCCCTCCCTCCCTCTCTC (hg19) ; chr4:g.5808177_5808178insTCCCTCCCTCCCTCTCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5808177_5808178insTCCCTCCCTCCCTCTCTC , CM000666.2:g.5808177_5808178insTCCCTCCCTCCCTCTCTC	GRCh38
NC_000004.11:g.5809904_5809905insTCCCTCCCTCCCTCTCTC , CM000666.1:g.5809904_5809905insTCCCTCCCTCCCTCTCTC	GRCh37
NC_000004.10:g.5860805_5860806insTCCCTCCCTCCCTCTCTC	NCBI36
NG_008843.1:g.101981_101982insTCCCTCCCTCCCTCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.2562-24_2562-23insTCCCTCCCTCCCTCTCTC (EVC) MANE Select	ENSP00000264956.6:n.2562-24_2562-23insTCCCTCCCTCCCTCTCTC
ENST00000264956.10:c.2562-24_2562-23insTCCCTCCCTCCCTCTCTC (EVC)	ENSP00000264956.6:n.2562-24_2562-23insTCCCTCCCTCCCTCTCTC
ENST00000506216.5:n.1647+17316_1647+17317insGAGAGAGGGAGGGAGGGA (CRMP1)
NM_001306090.1:c.2562-24_2562-23insTCCCTCCCTCCCTCTCTC (EVC)	NP_001293019.1:n.2562-24_2562-23insTCCCTCCCTCCCTCTCTC
NM_153717.2:c.2562-24_2562-23insTCCCTCCCTCCCTCTCTC (EVC)	NP_714928.1:n.2562-24_2562-23insTCCCTCCCTCCCTCTCTC
XM_006713865.2:c.2562-24_2562-23insTCCCTCCCTCCCTCTCTC (EVC)	XP_006713928.1:n.2562-24_2562-23insTCCCTCCCTCCCTCTCTC
XM_006713866.2:c.2562-24_2562-23insTCCCTCCCTCCCTCTCTC (EVC)	XP_006713929.1:n.2562-24_2562-23insTCCCTCCCTCCCTCTCTC
XR_427473.2:n.2752-24_2752-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_427475.2:n.2752-24_2752-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_427476.2:n.2752-24_2752-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924920.1:n.2752-24_2752-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924921.1:n.2752-24_2752-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924922.1:n.2752-24_2752-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924923.1:n.2752-24_2752-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924924.1:n.2752-24_2752-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924925.1:n.2752-24_2752-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924926.1:n.2752-24_2752-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924927.1:n.2752-24_2752-23insTCCCTCCCTCCCTCTCTC (EVC)
XM_006713865.3:c.2562-24_2562-23insTCCCTCCCTCCCTCTCTC (EVC)	XP_006713928.1:n.2562-24_2562-23insTCCCTCCCTCCCTCTCTC
XM_006713866.3:c.2562-24_2562-23insTCCCTCCCTCCCTCTCTC (EVC)	XP_006713929.1:n.2562-24_2562-23insTCCCTCCCTCCCTCTCTC
XR_001741164.1:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_001741165.1:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_001741166.1:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_001741167.1:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_001741168.1:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_001741169.2:n.2606-24_2606-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_001741170.1:n.2827-24_2827-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_001741171.1:n.2047-24_2047-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_427473.3:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_427475.3:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_427476.3:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924920.2:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924921.2:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924922.2:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924924.2:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924925.2:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
XR_924926.2:n.2742-24_2742-23insTCCCTCCCTCCCTCTCTC (EVC)
NM_153717.3:c.2562-24_2562-23insTCCCTCCCTCCCTCTCTC (EVC) MANE Select	NP_714928.1:n.2562-24_2562-23insTCCCTCCCTCCCTCTCTC
NM_001306090.2:c.2562-24_2562-23insTCCCTCCCTCCCTCTCTC (EVC)	NP_001293019.1:n.2562-24_2562-23insTCCCTCCCTCCCTCTCTC