Canonical Allele Identifier: CA356141964

Gene: EVC CRMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5793719T>G , CM000666.2:g.5793719T>G	GRCh38
NC_000004.11:g.5795446T>G , CM000666.1:g.5795446T>G	GRCh37
NC_000004.10:g.5846347T>G	NCBI36
NG_008843.1:g.87523T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_153717.3:c.1886+2T>G (EVC) MANE Select	NP_714928.1:n.1886+2T>G
ENST00000264956.11:c.1886+2T>G (EVC) MANE Select	ENSP00000264956.6:n.1886+2T>G
NM_001306090.1:c.1886+2T>G (EVC)	NP_001293019.1:n.1886+2T>G
NM_001306090.2:c.1886+2T>G (EVC)	NP_001293019.1:n.1886+2T>G
NM_153717.2:c.1886+2T>G (EVC)	NP_714928.1:n.1886+2T>G
ENST00000264956.10:c.1886+2T>G (EVC)	ENSP00000264956.6:n.1886+2T>G
ENST00000506216.5:n.1647+31775A>C (CRMP1)
ENST00000506240.1:n.204+2T>G (EVC)
ENST00000515113.1:n.110+2T>G (EVC)
XM_006713865.2:c.1886+2T>G (EVC)	XP_006713928.1:n.1886+2T>G
XM_006713865.3:c.1886+2T>G (EVC)	XP_006713928.1:n.1886+2T>G
XM_006713866.2:c.1886+2T>G (EVC)	XP_006713929.1:n.1886+2T>G
XM_006713866.3:c.1886+2T>G (EVC)	XP_006713929.1:n.1886+2T>G
XR_001741164.1:n.2066+2T>G (EVC)
XR_001741165.1:n.2066+2T>G (EVC)
XR_001741166.1:n.2066+2T>G (EVC)
XR_001741167.1:n.2066+2T>G (EVC)
XR_001741168.1:n.2066+2T>G (EVC)
XR_001741169.2:n.1930+2T>G (EVC)
XR_001741170.1:n.2068+2T>G (EVC)
XR_001741171.1:n.1371+2T>G (EVC)
XR_427473.2:n.2076+2T>G (EVC)
XR_427473.3:n.2066+2T>G (EVC)
XR_427475.2:n.2076+2T>G (EVC)
XR_427475.3:n.2066+2T>G (EVC)
XR_427476.2:n.2076+2T>G (EVC)
XR_427476.3:n.2066+2T>G (EVC)
XR_924920.1:n.2076+2T>G (EVC)
XR_924920.2:n.2066+2T>G (EVC)
XR_924921.1:n.2076+2T>G (EVC)
XR_924921.2:n.2066+2T>G (EVC)
XR_924922.1:n.2076+2T>G (EVC)
XR_924922.2:n.2066+2T>G (EVC)
XR_924923.1:n.2076+2T>G (EVC)
XR_924924.1:n.2076+2T>G (EVC)
XR_924924.2:n.2066+2T>G (EVC)
XR_924925.1:n.2076+2T>G (EVC)
XR_924925.2:n.2066+2T>G (EVC)
XR_924926.1:n.2076+2T>G (EVC)
XR_924926.2:n.2066+2T>G (EVC)
XR_924927.1:n.2076+2T>G (EVC)
XR_924928.1:n.2078+2T>G (EVC)