Canonical Allele Identifier: CA915943013

Gene: EVC CRMP1

Linked Data

• ClinVar Variation Id: 666179
• ClinVar RCV Id: RCV000824617
• dbSNP Id: rs1577663625

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5808198_5808223del , CM000666.2:g.5808198_5808223del	GRCh38
NC_000004.11:g.5809925_5809950del , CM000666.1:g.5809925_5809950del	GRCh37
NC_000004.10:g.5860826_5860851del	NCBI36
NG_008843.1:g.102002_102027del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.2562-3_2584del (EVC)
ENST00000264956.10:c.2562-3_2584del (EVC)
ENST00000506216.5:n.1647+17271_1647+17296del (CRMP1)
NM_001306090.1:c.2562-3_2584del (EVC)
NM_153717.2:c.2562-3_2584del (EVC)
XM_006713865.2:c.2562-3_2584del (EVC)
XM_006713866.2:c.2562-3_2584del (EVC)
XR_427473.2:n.2752-3_2774del (EVC)
XR_427475.2:n.2752-3_2774del (EVC)
XR_427476.2:n.2752-3_2774del (EVC)
XR_924920.1:n.2752-3_2774del (EVC)
XR_924921.1:n.2752-3_2774del (EVC)
XR_924922.1:n.2752-3_2774del (EVC)
XR_924923.1:n.2752-3_2774del (EVC)
XR_924924.1:n.2752-3_2774del (EVC)
XR_924925.1:n.2752-3_2774del (EVC)
XR_924926.1:n.2752-3_2774del (EVC)
XR_924927.1:n.2752-3_2774del (EVC)
XM_006713865.3:c.2562-3_2584del (EVC)
XM_006713866.3:c.2562-3_2584del (EVC)
XR_001741164.1:n.2742-3_2764del (EVC)
XR_001741165.1:n.2742-3_2764del (EVC)
XR_001741166.1:n.2742-3_2764del (EVC)
XR_001741167.1:n.2742-3_2764del (EVC)
XR_001741168.1:n.2742-3_2764del (EVC)
XR_001741169.2:n.2606-3_2628del (EVC)
XR_001741170.1:n.2827-3_2849del (EVC)
XR_001741171.1:n.2047-3_2069del (EVC)
XR_427473.3:n.2742-3_2764del (EVC)
XR_427475.3:n.2742-3_2764del (EVC)
XR_427476.3:n.2742-3_2764del (EVC)
XR_924920.2:n.2742-3_2764del (EVC)
XR_924921.2:n.2742-3_2764del (EVC)
XR_924922.2:n.2742-3_2764del (EVC)
XR_924924.2:n.2742-3_2764del (EVC)
XR_924925.2:n.2742-3_2764del (EVC)
XR_924926.2:n.2742-3_2764del (EVC)
NM_153717.3:c.2562-3_2584del (EVC)
NM_001306090.2:c.2562-3_2584del (EVC)