Canonical Allele Identifier: CA356150462

Gene: EVC CRMP1

Linked Data

• dbSNP Id: rs1230001139
• gnomAD v3: 4-5808223-T-G
• gnomAD v4: 4-5808223-T-G
• MyVariant Identifiers: chr4:g.5809950T>G (hg19) ; chr4:g.5808223T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5808223T>G , CM000666.2:g.5808223T>G	GRCh38
NC_000004.11:g.5809950T>G , CM000666.1:g.5809950T>G	GRCh37
NC_000004.10:g.5860851T>G	NCBI36
NG_008843.1:g.102027T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.2584T>G (EVC) MANE Select	ENSP00000264956.6:p.Phe862Val
ENST00000264956.10:c.2584T>G (EVC)	ENSP00000264956.6:p.Phe862Val
ENST00000506216.5:n.1647+17271A>C (CRMP1)
NM_001306090.1:c.2584T>G (EVC)	NP_001293019.1:p.Phe862Val
NM_153717.2:c.2584T>G (EVC)	NP_714928.1:p.Phe862Val
XM_006713865.2:c.2584T>G (EVC)	XP_006713928.1:p.Phe862Val
XM_006713866.2:c.2584T>G (EVC)	XP_006713929.1:p.Phe862Val
XR_427473.2:n.2774T>G (EVC)
XR_427475.2:n.2774T>G (EVC)
XR_427476.2:n.2774T>G (EVC)
XR_924920.1:n.2774T>G (EVC)
XR_924921.1:n.2774T>G (EVC)
XR_924922.1:n.2774T>G (EVC)
XR_924923.1:n.2774T>G (EVC)
XR_924924.1:n.2774T>G (EVC)
XR_924925.1:n.2774T>G (EVC)
XR_924926.1:n.2774T>G (EVC)
XR_924927.1:n.2774T>G (EVC)
XM_006713865.3:c.2584T>G (EVC)	XP_006713928.1:p.Phe862Val
XM_006713866.3:c.2584T>G (EVC)	XP_006713929.1:p.Phe862Val
XR_001741164.1:n.2764T>G (EVC)
XR_001741165.1:n.2764T>G (EVC)
XR_001741166.1:n.2764T>G (EVC)
XR_001741167.1:n.2764T>G (EVC)
XR_001741168.1:n.2764T>G (EVC)
XR_001741169.2:n.2628T>G (EVC)
XR_001741170.1:n.2849T>G (EVC)
XR_001741171.1:n.2069T>G (EVC)
XR_427473.3:n.2764T>G (EVC)
XR_427475.3:n.2764T>G (EVC)
XR_427476.3:n.2764T>G (EVC)
XR_924920.2:n.2764T>G (EVC)
XR_924921.2:n.2764T>G (EVC)
XR_924922.2:n.2764T>G (EVC)
XR_924924.2:n.2764T>G (EVC)
XR_924925.2:n.2764T>G (EVC)
XR_924926.2:n.2764T>G (EVC)
NM_153717.3:c.2584T>G (EVC) MANE Select	NP_714928.1:p.Phe862Val
NM_001306090.2:c.2584T>G (EVC)	NP_001293019.1:p.Phe862Val